DOCSLIB.ORG

Vol. 81 Tuesday, No. 55 March 22, 2016 Pages 15153–15416

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Vol. 81 Tuesday, No. 55 March 22, 2016 Pages 15153–15416 Vol. 81 Tuesday, No. 55 March 22, 2016 Pages 15153–15416 OFFICE OF THE FEDERAL REGISTER VerDate Sep 11 2014 17:56 Mar 21, 2016 Jkt 238001 PO 00000 Frm 00001 Fmt 4710 Sfmt 4710 E:\FR\FM\22MRWS.LOC 22MRWS asabaliauskas on DSK3SPTVN1PROD with FRONTMATTER II Federal Register / Vol. 81, No. 55 / Tuesday, March 22, 2016 The FEDERAL REGISTER (ISSN 0097–6326) is published daily, SUBSCRIPTIONS AND COPIES Monday through Friday, except official holidays, by the Office PUBLIC of the Federal Register, National Archives and Records Administration, Washington, DC 20408, under the Federal Register Subscriptions: Act (44 U.S.C. Ch. 15) and the regulations of the Administrative Paper or fiche 202–512–1800 Committee of the Federal Register (1 CFR Ch. I). The Assistance with public subscriptions 202–512–1806 Superintendent of Documents, U.S. Government Publishing Office, Washington, DC 20402 is the exclusive distributor of the official General online information 202–512–1530; 1–888–293–6498 edition. Periodicals postage is paid at Washington, DC. Single copies/back copies: The FEDERAL REGISTER provides a uniform system for making Paper or fiche 202–512–1800 available to the public regulations and legal notices issued by Assistance with public single copies 1–866–512–1800 Federal agencies. These include Presidential proclamations and (Toll-Free) Executive Orders, Federal agency documents having general FEDERAL AGENCIES applicability and legal effect, documents required to be published Subscriptions: by act of Congress, and other Federal agency documents of public interest. Assistance with Federal agency subscriptions: Documents are on file for public inspection in the Office of the Email [email protected] Federal Register the day before they are published, unless the Phone 202–741–6000 issuing agency requests earlier filing. For a list of documents currently on file for public inspection, see www.ofr.gov. The seal of the National Archives and Records Administration authenticates the Federal Register as the official serial publication established under the Federal Register Act. Under 44 U.S.C. 1507, the contents of the Federal Register shall be judicially noticed. The Federal Register is published in paper and on 24x microfiche. It is also available online at no charge at www.fdsys.gov, a service of the U.S. Government Publishing Office. The online edition of the Federal Register is issued under the authority of the Administrative Committee of the Federal Register as the official legal equivalent of the paper and microfiche editions (44 U.S.C. 4101 and 1 CFR 5.10). It is updated by 6:00 a.m. each day the Federal Register is published and includes both text and graphics from Volume 59, 1 (January 2, 1994) forward. For more information, contact the GPO Customer Contact Center, U.S. Government Publishing Office. Phone 202-512-1800 or 866-512- 1800 (toll free). E-mail, gpocusthelp.com. The annual subscription price for the Federal Register paper edition is $749 plus postage, or $808, plus postage, for a combined Federal Register, Federal Register Index and List of CFR Sections Affected (LSA) subscription; the microfiche edition of the Federal Register including the Federal Register Index and LSA is $165, plus postage. Six month subscriptions are available for one-half the annual rate. The prevailing postal rates will be applied to orders according to the delivery method requested. The price of a single copy of the daily Federal Register, including postage, is based on the number of pages: $11 for an issue containing less than 200 pages; $22 for an issue containing 200 to 400 pages; and $33 for an issue containing more than 400 pages. Single issues of the microfiche edition may be purchased for $3 per copy, including postage. Remit check or money order, made payable to the Superintendent of Documents, or charge to your GPO Deposit Account, VISA, MasterCard, American Express, or Discover. Mail to: U.S. Government Publishing Office—New Orders, P.O. Box 979050, St. Louis, MO 63197-9000; or call toll free 1-866-512-1800, DC area 202-512-1800; or go to the U.S. Government Online Bookstore site, see bookstore.gpo.gov. There are no restrictions on the republication of material appearing in the Federal Register. How To Cite This Publication: Use the volume number and the page number. Example: 81 FR 12345. Postmaster: Send address changes to the Superintendent of Documents, Federal Register, U.S. Government Publishing Office, Washington, DC 20402, along with the entire mailing label from the last issue received. VerDate Sep 11 2014 17:56 Mar 21, 2016 Jkt 238001 PO 00000 Frm 00002 Fmt 4710 Sfmt 4710 E:\FR\FM\22MRWS.LOC 22MRWS asabaliauskas on DSK3SPTVN1PROD with FRONTMATTER III Contents Federal Register Vol. 81, No. 55 Tuesday, March 22, 2016 Agriculture Department Drug Enforcement Administration See Animal and Plant Health Inspection Service PROPOSED RULES See Forest Service Schedules of Controlled Substances: Placement of UR–144, XLR11, and AKB48 into Schedule Animal and Plant Health Inspection Service I; Correction, 15188–15190 RULES Black Stem Rust: Education Department Additions of Rust-Resistant Species and Varieties, 15153 NOTICES Agency Information Collection Activities; Proposals, Centers for Disease Control and Prevention Submissions, and Approvals: NOTICES National Longitudinal Transition Study 2012 Phase II, Meetings: 15289–15290 Advisory Council for the Elimination of Tuberculosis, Applications for New Awards: 15305–15306 Fulbright-Hays Doctoral Dissertation Research Abroad Disease, Disability, and Injury Prevention and Control Fellowship Program, 15290–15295 Special Emphasis Panel, 15305–15309 Requests for Nominations: Energy Department Board of Scientific Counselors, National Center for See Federal Energy Regulatory Commission Environmental Health/Agency for Toxic Substances NOTICES and Disease Registry, 15308 Applications to Export Electric Energy: Tenaska Energia de Mexico, S. de R.L. de C.V., 15295 Coast Guard Design of a Consent-Based Siting Process for Nuclear Waste NOTICES Storage and Disposal Facilities: Agency Information Collection Activities; Proposals, Extension of Comment Period, 15295–15296 Submissions, and Approvals, 15323–15326 Meetings: Environmental Protection Agency National Boating Safety Advisory Council, 15324–15325 PROPOSED RULES Port Access Route Study: Air Quality State Implementation Plans; Approvals and Nantucket Sound, 15327–15328 Promulgations: Removal of Conditions of Entry on Vessels Arriving from Arizona; Infrastructure Requirements to Address the Republic of Cuba, 15326–15327 Interstate Transport for the 2008 Ozone NAAQS, Requests for Nominations: 15200–15205 National Boating Safety Advisory Council, 15326 Mississippi; Air Plan Disapprovals; Prong 42008 Ozone, 2010 NO2, SO2, and 2012 PM2.5, 15205–15210 Commerce Department See International Trade Administration Federal Aviation Administration See National Oceanic and Atmospheric Administration RULES Airworthiness Directives: Commodity Futures Trading Commission Turbomeca S.A. Turboshaft Engines, 15154–15156 NOTICES PROPOSED RULES Comparability Determination for the European Union: Airworthiness Directives: Dually-Registered Derivatives Clearing Organizations and Agusta S.p.A. Helicopters, 15171–15173 Central Counterparties, 15260–15272 NOTICES Environmental Assessments; Availability, etc.: Community Living Administration Proposed Airport Traffic Control Tower and Base NOTICES Building at Peoria International Airport, Peoria, IL, Agency Information Collection Activities; Proposals, 15400 Submissions, and Approvals: Requests to Release Airport Properties, 15400–15401 National Maltreatment Reporting System, 15309–15310 Waivers for Aeronautical Land-Use Assurances: Big Spring McMahon-Wrinkle Airport, Big Spring, TX, Defense Department 15401 NOTICES Mankato Regional Airport, Mankato, MN, 15399–15400 Agency Information Collection Activities; Proposals, Submissions, and Approvals: Federal Communications Commission Bid Guarantees, Performance and Payment Bonds, and PROPOSED RULES Alternative Payment Protections, 15304–15305 Radio Broadcasting Services: Contractors Performing Private Security Functions Maryville, MO, 15216–15217 Outside the United States, 15303–15304 Unlicensed White Space Devices, 15210–15216 Drug–Free Workplace, 15303 Manual for Courts-Martial; Amendments to Part IV Federal Energy Regulatory Commission Discussion and Appendix 22, 15278–15289 RULES Manual for Courts-Martial; Proposed Amendments, 15272– Standards for Business Practices of Interstate Natural Gas 15278 Pipelines; Correction, 15156–15159 VerDate Sep<11>2014 18:25 Mar 21, 2016 Jkt 238001 PO 00000 Frm 00001 Fmt 4748 Sfmt 4748 E:\FR\FM\22MRCN.SGM 22MRCN asabaliauskas on DSK3SPTVN1PROD with FRONTMATTER IV Federal Register / Vol. 81, No. 55 / Tuesday, March 22, 2016 / Contents NOTICES Forest Service Agency Information Collection Activities; Proposals, NOTICES Submissions, and Approvals, 15300–15302 Environmental Impact Statements; Availability, etc.: Applications: Shasta-Trinity National Forest; California; Lower Grand River Dam Authority, 15296–15297 McCloud Fuels Management, 15220–15222 Combined Filings, 15297–15300 General Services Administration Federal Motor Carrier Safety Administration NOTICES PROPOSED RULES Agency Information Collection Activities; Proposals, Hours of Service of Drivers; Parts and Accessories: Submissions, and Approvals: ArcelorMittal Indiana Harbor, LLC; Application for Bid Guarantees, Performance and Payment Bonds, and Exemptions, 15217–15219 Alternative Payment
Load more

Recommended publications
  • Comparative Durability and Abrasion Resistance of Natural and Synthetic
    Comparative Durability and Abrasion Resistance of Natural and Synthetic Latex Gloves Ryan Michel2 and Katrina Cornish1,2 Department of Horticulture and Crop Science, 2Department of Food, Agricultural and Biological Engineering, Ohio Agricultural Research and Development Center, The Ohio State University, Wooster, OH 44691 Abstract Medical gloves assist with the prevention of the spread of germs and are required to be worn when working with blood, body tissues, mucous membrane, and broken skin. They should provide good protection between hands and bio hazardous fluids to prevent contamination and promote safety of all healthcare workers and patients. Hence, it is critical for medical gloves to meet a standard performance criterion. Under ASTM D 3577 and D 3578, medical gloves have requirements they must meet in order to be sold and distributed as new gloves. However, there are no industry standards for gloves to meet while in use. The goal of this project was to develop a standard test for glove durability after their initial use. For the tests, gloves were worn by a mechanized prosthetic hand that was put under different conditions which are normally experienced by professionals in the medical field. This design was developed and later confirmed by Dr. Katrina Cornish: Design: Effects of media outside the glove Phosphate buffered saline (PBS), 70% ethanol, air Gloves Tested: Chloroprene, Latex 2, Nitrile, Polyvinyl Chloride and Latex 1 To evaluate glove durability during use, the gloves were immersed in different media before being subjected to contact with an abrasive surface. From this design, ranking of commercially available gloves are developed based on the time until failure of the gloves in these tests.
    [Show full text]
  • Medical Glove Guidance Manual
    On December 19, 2016, the FDA published a final rule banning powdered gloves based on the unreasonable and substantial risk of illness or injury to individuals exposed to the powdered gloves (https://www.federalregister.gov/documents/2016/12/19/2016- 30382/banned-devices-powdered-surgeons-gloves-powdered-patient- examination-gloves-and-absorbable-powder). This guidance document has not been updated to reflect the ban. FDA is assessing how to revise this guidance to represent our current thinking on medical gloves. Guidance for Industry and FDA Staff Medical Glove Guidance Manual Document issued on January 22, 2008 This document supersedes Guidance for Medical Gloves – A Workshop Manual, September 30, 1996. For questions regarding this document contact the Infection Control Devices Branch Chief at (301) 796-5580. U.S. Department of Health and Human Services Food and Drug Administration Center for Devices and Radiological Health Office of Device Evaluation Division of Anesthesiology, General Hospital, Infection Control, and Dental Devices Infection Control Devices Branch Preface Public Comment You may submit electronic comments and suggestions at any time for Agency consideration to http://www.regulations.gov. Submit written comments to the Division of Dockets Management, Food and Drug Administration, 5630 Fishers Lane, Room 1061, (HFA-305), Rockville, MD 20852. Identify all comments with the docket number listed in the notice of availability that publishes in the Federal Register. Comments may not be acted upon by the Agency until the document is next revised or updated. Additional Copies Additional copies are available from the Internet. You may also send an e-mail request to [email protected] to receive a copy of the guidance.
    [Show full text]
  • Elastomeric Film Products with Improved Chemical Resistance
    Office europeen des brevets (fi) Publication number : 0 524 836 A1 @ EUROPEAN PATENT APPLICATION @ Application number: 92306810.0 @ Int. CI.5: C08L 9/04, C08L 13/02, C08J 5/02 (22) Date of filing : 24.07.92 (§) Priority : 26.07.91 US 736369 @ Inventor : Miller, Robert G. 73 Cherrystone Drive Willowdale, Ontario M2H 1S2 (CA) @ Date of publication of application : Inventor : MacKillop, Duncan A. 27.01.93 Bulletin 93/04 61 Hernshaw Crescent Etobicoke, Ontario M9C 3M6 (CA) Inventor : Tankovitz, Oskar @ Designated Contracting States : 85 Thorncliffe Park Drive, Suite 2606 BE DE DK ES FR GB GR IT LU NL PT Toronto M4H 1L6 (CA) (71) Applicant : ORTHO PHARMACEUTICAL © Representative : Fisher, Adrian John et al CORPORATION CARPMAELS & RANSFORD 43 Bloomsbury U.S. Route 202 P.O. Box 300 Square Raritan New Jersey 08869-0602 (US) London WC1A 2RA (GB) (54) Elastomeric film products with improved chemical resistance. (57) A latex film product such as a prophylactic condom, a surgical glove, a medical examination glove, and the like, having improved chemical resistance, such product comprising a shaped film consisting essentially of a cured mixture of (a) a copolymer of acrylonitrile and butadiene or isoprene, and (b) a high styrene content styrene-butadiene copolymer. < CO CO 00 LU Jouve, 18, rue Saint-Denis, 75001 PARIS EP 0 524 836 A1 The invention relates to elastomeric film products such as prophylactic condoms and surgical gloves made from certain acrylonitrile containing synthetic latexes. Background of the Invention 5 Commercial condoms have been manufactured from natural rubber (NR) latexfor over sixty years. NRIatex is an excellent material for the latex dipping process customarily employed for producing such articles as con- doms, medical gloves, and the like, since it is stable and can readily be compounded with aqueous dispersions of curatives, e.g.
    [Show full text]
  • A Critical Review of the Assessment of Medical Gloves
    This is a repository copy of A critical review of the assessment of medical gloves. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/157053/ Version: Accepted Version Article: Preece, D., Lewis, R. orcid.org/0000-0002-4300-0540 and Carre, M.J. (2020) A critical review of the assessment of medical gloves. Tribology: Materials, Surfaces and Interfaces. ISSN 1751-5831 https://doi.org/10.1080/17515831.2020.1730619 This is an Accepted Manuscript of an article published by Taylor & Francis in Tribology: Materials, Surfaces and Interfaces on 23 Feb 2020, available online: http://www.tandfonline.com/10.1080/17515831.2020.1730619. Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ A Critical Review of the Assessment of Medical Gloves D. Preecea*, R. Lewis and M. J. Carré aDepartment of Mechanical Engineering, University of Sheffield, Sheffield, United Kingdom; *[email protected] Abstract Medical protective gloves must be assessed to adequate standards before becoming available for commercial use.
    [Show full text]
  • Investigation of Neoprene Medical Gloves: Analysis of Material Properties, Durability, and Bacterial Barrier Efficacy
    University of Connecticut OpenCommons@UConn Honors Scholar Theses Honors Scholar Program Summer 6-8-2020 Investigation of Neoprene Medical Gloves: Analysis of Material Properties, Durability, and Bacterial Barrier Efficacy Amanda Agui University of Connecticut - Storrs, [email protected] Follow this and additional works at: https://opencommons.uconn.edu/srhonors_theses Part of the Biology and Biomimetic Materials Commons, and the Polymer and Organic Materials Commons Recommended Citation Agui, Amanda, "Investigation of Neoprene Medical Gloves: Analysis of Material Properties, Durability, and Bacterial Barrier Efficacy" (2020). Honors Scholar Theses. 649. https://opencommons.uconn.edu/srhonors_theses/649 Investigation of Neoprene Medical Gloves: Analysis of Material Properties, Durability, and Bacterial Barrier Efficacy Amanda Agui June 8, 2020 Department: University of Connecticut - Materials Science and Engineering Honors Thesis Committee: Honors Advisor and Thesis Advisor: Dr. Seok-Woo Lee, University of Connecticut Materials Science and Engineering Department 1. Abstract This work aims to investigate the material properties, durability, and bacterial barrier efficacy of neoprene for applications in the healthcare/medical field. A special focus on material stiffness and fatigue failure will be explored. Additionally, manufacturer regulations and testing will be inspected to ensure medical gloves made of neoprene blends have a proper lifespan for its desired application in the healthcare community. The resistance of protective gloves and its ability to withstand perforation failure will be investigated to guarantee the safety of users holds extreme importance. Lastly, an analysis of the bacterial barrier efficacy of neoprene gloves will be determined. 1 2. Introduction Medical examination and surgical gloves protect users from the risk of contamination [1]. Due to the current climate of COVID-19, as well as increasing latex allergy concerns, the research and development of synthetic gloves made of non-latex materials is observed.
    [Show full text]
  • Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings Last Update: July 2019
    Accessable version: https://www.cdc.gov/infectioncontrol/guidelines/isolation/index.html 2007 Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings Last update: July 2019 Jane D. Siegel, MD; Emily Rhinehart, RN MPH CIC; Marguerite Jackson, PhD; Linda Chiarello, RN MS; the Healthcare Infection Control Practices Advisory Committee Acknowledgement: The authors and HICPAC gratefully acknowledge Dr. Larry Strausbaugh for his many contributions and valued guidance in the preparation of this guideline. Suggested citation: Siegel JD, Rhinehart E, Jackson M, Chiarello L, and the Healthcare Infection Control Practices Advisory Committee, 2007 Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings https://www.cdc.gov/infectioncontrol/guidelines/isolation/index.html Page 1 of 206 Guideline for Isolation Precautions: Preventing Transmission of Infectious Agents in Healthcare Settings (2007) Healthcare Infection Control Practices Advisory Committee (HICPAC): Chair PERROTTA, Dennis M. PhD., CIC Patrick J. Brennan, MD Adjunct Associate Professor of Epidemiology Professor of Medicine University of Texas School of Public Health Division of Infectious Diseases Texas A&M University School of Rural Public University of Pennsylvania Medical School Health Executive Secretary PITT, Harriett M., MS, CIC, RN Michael Bell, MD Director, Epidemiology Division of Healthcare Quality Promotion Long Beach Memorial Medical Center National Center for Infectious Diseases
    [Show full text]
  • Guayule Rubber Medical Radiation Attenuation Glove Zhenyu Li1 and Katrina Cornish2 1
    Guayule rubber medical radiation attenuation glove Zhenyu Li1 and Katrina Cornish2 1. EnergyEne Inc, Wooster, OH; 2. Department of Food, Agriculture and Biological Engineering, The Ohio State University, Columbus, OH 1 Introduction Radiation attenuation (RA) gloves protect and shield health care professionals (HCP) from occupational exposure to ionizing radiation. Potential end-users include radiologists, cardiologists, surgeons, and technicians who administer radiation examinations and/or perform radiation treatments. The number and types of procedures involved with radiation exposure to HCP in 2006 are shown in Table 1, and this number totaled over 16 million in 2014 in the US (2). Some fluoroscopy-assisted surgeries require the hands of the HCP to be in or near the primary radiation field. Therefore, of all body parts, the hands usually receive the highest cumulative levels of radiation (3-8). The Nuclear Regulatory Commission (NRC) limits the maximum permissible exposure for the hands to 500 mSv/year, while most institutions establish a conservative safety threshold of 50 mSv/year to maintain the exposures As Low As Reasonably Achievable (ALARA). The ALARA level is frequently exceeded for radiation workers in high risk areas (3). Various simulated and real clinical studies reported operators’ hand doses range from 30-80 μSv/min to over 500 μSv/min (4, 7). This translates to only 17 hrs of exposure to 500 μSv/min, 104 h to 80 μSv/min and 278 hrs to 30 μSv/min before the maximum permissible exposure level (500 mSv/year) is reached, all clearly much less than the work load of a practitioner. Hand exposure Table 1.
    [Show full text]
  • (93/42/Eec) in Relation to Medical Devices Containing Natural Rubber Latex
    EUROPEAN COMMISSION ENTERPRISE DIRECTORATE-GENERAL Single Market : regulatory environment, standardisation and New Approach Pressure equipment, medical devices, metrology MEDDEV. 2.5/9 rev.1 February 2004 GUIDELINES ON MEDICAL DEVICES IMPLICATIONS OF THE MEDICAL DEVICES DIRECTIVES (93/42/EEC) IN RELATION TO MEDICAL DEVICES CONTAINING NATURAL RUBBER LATEX: A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES Note The present Guidelines are part of a set of Guidelines relating to questions of application of EC-Directives on medical devices. They are legally not binding. The Guidelines have been carefully drafted through a process of intensive consultation of the various interest parties (competent authorities, Commission services, industries, other interested parties) during which intermediate drafts were circulated and comments were taken up in the document. Therefore, this document reflects positions taken by representatives of interest parties in the medical devices sector. 1 Background and Scope Due to the combination of its superior barrier qualities, strength, flexibility and comfort, natural rubber latex (NRL) has been increasingly used in a variety of medical devices. In particular, the properties of NRL make it a preferred material for medical gloves. The clinical use of latex gloves has increased considerably during the last 20 years, due mainly to escalating risks associated with blood-borne infectious agents. The main function of these gloves is to create a protective barrier between the patient and health care worker and also to facilitate general hand hygiene. In response to the growing apprehension surrounding medical devices containing NRL, the Directorate General for Enterprise of the European Commission presented questions to the Scientific Committee on Medicinal Products and Medical Devices (SCMPMD).
    [Show full text]
  • Top Clinical Concerns Related to Surgical Gloves
    Top Clinical Concerns Related to Surgical Gloves William Halstead, M.D., the great surgical innovator, introduced sterilized surgical gloves in the late 19th century, saving countless lives over many generations. Gloving material and techniques have advanced considerably since then, especially in recent years as knowledge of how to maximize safety for patients and health professionals has advanced. This article summarizes recent surgical glove innovations, relevant research and current best practices for surgical gloving. It further discusses trade-offs and concerns common in operating rooms transitioning from older gloving practices to newer, safer ones. Best Practice Trend #1: Synthetic gloves Reports of latex allergies attracted attention in the The use of latex surgical gloves is on the 1980s. The first fatal reaction was reported in 1991.1 decline, yet, in 2015, latex gloves still % Johns Hopkins Hospital, where latex surgical gloves accounted for nearly half of surgical gloves 8-12 were first used, banned their use altogether in 2008.2 sold in the United States.5 Historically, of healthcare workers are 3 gloves made with natural rubber latex have affected by latex sensitivity. Allergic reactions to latex are triggered by proteins been popular because of their comfortable found in natural rubber latex and mediated by the IgE fit and feel. The decline of latex gloves antibody. Touching latex or inhaling particles shed from sales has been accelerated, in part, by gloves can cause a reaction. Sensitivity increases over technological improvements to make time and with repeated use. This makes health care synthetic gloves more closely mimic the fit, No treatment exists professionals vulnerable.
    [Show full text]
  • Glove Coating and Manufacturing Process
    (19) TZZ 58__ZZ_T (11) EP 2 581 100 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 17.04.2013 Bulletin 2013/16 A61L 31/10 (2006.01) C08J 7/04 (2006.01) (21) Application number: 13150983.8 (22) Date of filing: 08.02.2008 (84) Designated Contracting States: • Wamg, Shiping AT BE BG CH CY CZ DE DK EE ES FI FR GB GR Libertyville, IL Illinois 60048 (US) HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT • Chen, Seong Fong RO SE SI SK TR 11700 Gelugor, Penang (MY) • Chong, Chaung Sim (30) Priority: 08.02.2007 US 672705 14000 Burkit Mertajam, Seberang Peraj (MY) (62) Document number(s) of the earlier application(s) in (74) Representative: Barchielli, Giovanna accordance with Art. 76 EPC: Bianchetti Bracco Minoja S.r.l. 08725350.6 / 2 121 200 Via Plinio, 63 20129 Milano (IT) (71) Applicant: Allegiance Corporation Mcgaw Park IL 60064 (US) Remarks: This application was filed on 11-01-2013 as a (72) Inventors: divisional application to the application mentioned • Wong, Wei Cheong under INID code 62. Kedah (MY) (54) Glove coating and manufacturing process (57) This invention relates to a method for preparing coating of the invention is formed from synthetic polyiso- an elastomeric article with improved lubricity and donna- prene rubber that may or may not contain minor amounts bility and reduced stickiness/tackiness. According to the of other components. The coating is preferably directly methods of the invention, the internal surface of the elas- bonded to the underlying elastomenc article.
    [Show full text]
  • Clinical Issue
    ISSUE 4 THE CLINICAL ISSUE DOES THE GLOVE FIT? CRITICAL CONSIDERATIONS FOR THE SELECTION OF MEDICAL GLOVES INTRODUCTION Medical gloves are considered one of the most critical components of barrier protection for those who are exposed to infectious substances and hazardous materials. Whether facing the demands of routine patient care, antibiotic resistance, threats of bioterrorism, or other challenges, healthcare personnel must have appropriate personal protective equipment, including gloves, and be able to rely on that protection throughout the performance of their tasks. Indeed, the Centers for Disease Control TABLE OF CONTENTS: and Prevention (CDC), the Occupational Safety and Health Administration (OSHA), and the National Institute for Introduction..................................1 Occupational Safety and Health (NIOSH) all stress the importance of appropriate glove selection.1,2,3 Physical Characteristics ............ 2 Questions that should be asked when selecting medical Associated Complications ........6 gloves include: Does the glove chosen fit the task at hand? Environmental Impact .............10 What physical glove characteristics should be evaluated? Conclusion ................................ 12 What potential complications might be experienced when using gloves? Should the environmental impact of glove disposal be a concern? These are all issues that must be considered for appropriate glove selection. Kathleen Stoessel, RN, BSN, MS Susan M. Smith, BA CLEANING REUSABLE MEDICAL DEVICES: A CRITICAL FIRST STEP PHYSICAL CHARACTERISTICS
    [Show full text]
  • Opinion on the Protection Offered by Natural Rubber Latex Medical
    EUROPEAN COMMISSION HEALTH & CONSUMER PROTECTION DIRECTORATE-GENERAL Directorate C - Public Health and Risk Assessment C7 - Risk assessment Brussels, C7/SANCO/SCMPMD/2003/00023 final D(03) OPINION OF THE SCIENTIFIC COMMITTEE ON MEDICINAL PRODUCTS AND MEDICAL DEVICES ON “THE PROTECTION OFFERED BY NATURAL RUBBER LATEX MEDICAL DEVICES (MEDICAL GLOVES AND CONDOMS) AGAINST TRANSMISSIBLE DISEASES” Adopted by the SCMPMD during the 24th plenary meeting of 16 October 2003 OPINION OF THE SCIENTIFIC COMMITTEE ON MEDICINAL PRODUCTS AND MEDICAL DEVICES ON “THE PROTECTION OFFERED BY NATURAL RUBBER LATEX MEDICAL DEVICES (MEDICAL GLOVES AND CONDOMS) AGAINST TRANSMISSIBLE DISEASES” Adopted by the SCMPMD during the 24th plenary meeting of 16 October 2003 TABLE OF CONTENTS 1. Introduction to the problem 2. Mandate 3. Background 4. Physical properties of natural rubber latex medical products used for personal protection and alternative materials 5. Background information on viruses and TSE 6. Barrier effectiveness of gloves 7. Risk assessment including populations at risk 8. Conclusions/recommendations 9. References 2 1. Introduction to the problem The changing characteristics of the risk of infection by blood borne pathogens with respect to clinical procedures has resulted in a number of discussions about the effectiveness of protective equipment and materials, including natural rubber latex products such as medical gloves, designed to have this barrier function (Anonymous 1987, CDC 1988, Fay and Dooher1992, Fay 1996, FDA 1999, Gerberding et al 1995, Rabussay and Korniewicz 1997, Stringer et al 2001). In addition, the low quality of some surgical and examination gloves, considering the importance of the barrier effectiveness, has been a concern in the past (Fay and Dooher 1992).
    [Show full text]