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YY 0285.1-2004 PDF in English


YY 0285.1-2004 (YY0285.1-2004) PDF English
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YY 0285.1-2004English70 Add to Cart 0-9 seconds. Auto-delivery. Sterile, single-use intravascular catheters. Part 1: General requirements Obsolete
YY 0285.1-2017English185 Add to Cart 0-9 seconds. Auto-delivery. Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements Valid
Newer version: YY 0285.1-2017    Standards related to: YY 0285.1-2017
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YY 0285.1-2004: PDF in English

YY 0285.1-2004 YY PHARMACEUTICAL INDUSTRY STANDARD OF THE PEOPLE’S REPUBLIC OF CHINA ICS 11.040.20 C 31 YY 0285.1-2004 / ISO 10555-1.1995 Replacing YY 0285.1-1999 Sterile, single-use intravascular catheters – Part 1. General requirements ISSUED ON. JULY 16, 2004 IMPLEMENTED ON. AUGUST 1, 2005 Issued by. China Food and Drug Administration Table of Contents Foreword ... 3  1 Scope ... 4  2 Normative references ... 4  3 Definitions ... 4  4 Requirements ... 6  5 Designation of nominal size ... 8  6 Information to be supplied by manufacturer ... 8  Annex A (Informative) Test method for corrosion resistance ... 10  Annex B (Normative) Method for determining force at break ... 11  Annex C (Normative) Test method for liquid leakage under pressure ... 13  Annex D (Normative) Test method for air leakage into hub assembly during aspiration ... 15  Bibliography ... 17  Foreword This Part of YY 0285 identically uses the International Standard ISO 10555-1.1995 and ISO 10555-1/Amendment 1-1999 Sterile, single-use intravascular catheters - Part 1. General requirements. Meanwhile, it is also the revision to YY 0285.1-1999. This edition and main technical differences of YY 0285.1-1999 are mainly based on ISO 10555-1 Amendment 1-1999. It added the relevant requirements for hydrated ducts. Requirements of clause 5 of this Part are recommendatory. Annex A ~ Annex D of this Part are normative. This Part was proposed by National Technical Committee on Medical Infusion Equipment of Standardization Administration of China. This Part shall be under the jurisdiction of State Drug Administration Jinan Medical Device Quality Supervision and Inspection Center. Main drafting organization of this Part. Shandong Medical Equipment Product Quality Inspection Center. Main drafters of this Part. Wang Yanwei, Wu Ping, Qian Chengyu. Sterile, single-use intravascular catheters – Part 1. General requirements 1 Scope This Part of YY 0285 specifies general requirements for intravascular catheters, supplied in the sterile condition and intended for single use, for any application. It does not apply to intravascular catheter accessories, which will be covered by a separate standard. NOTE Requirements for accessories are specified in YY 0450. 2 Normative references The provisions in following documents become the provisions of this Part through reference in this Part. For dated references, the subsequent amendments (excluding corrigendum) or revisions do not apply to this Part, however, parties who reach an agreement based on this Part are encouraged to study if the latest versions of these documents are applicable. For undated references, the latest edition of the referenced document applies. GB/T 1962, The conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment (idt ISO 594) GB 15810, Sterile hypodermic syringes for single use (GB 15810-1995, eqv ISO 7886-1.1993) 3 Definitions For the purposes of this document, the following definitions apply. 3.1 intravascular catheter tubular device single or multilumen, designed to be partially or totally inserted or implanted into the cardiovascular system for diagnostic and/or therapeutic purposes 3.2 distal end Bibliography [1] GB/T 16886.1-2001, Biological evaluation of medical devices - Part 1. Evaluation and testing (idt ISO 10993-1997) [2] GB 18278-2000, Sterilization of health care products - Requirements for validation and routine control--Industrial moist heat sterilization (idt ISO 11134.1994) [3] GB 18279-2000, Biological evaluation of medical devices - Part 1. Evaluation and testing (idt 11135.1994) [4] GB 18280-2000, Sterilization of health care products - Requirement for validation and routine control--Radiation sterilization (idt 11137.1995) ......
Source: Above contents are excerpted from the PDF -- translated/reviewed by: www.chinesestandard.net / Wayne Zheng et al.