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YY/T 1119-2008 English PDF

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YY/T 1119-2008: Terminology relating to medical polymer products
Status: Valid

YY/T 1119: Evolution and historical versions

Standard IDContents [version]USDSTEP2[PDF] delivered inStandard Title (Description)StatusPDF
YY/T 1119-2008English509 Add to Cart 4 days [Need to translate] Terminology relating to medical polymer products Valid YY/T 1119-2008
YY/T 1119-1999English519 Add to Cart 4 days [Need to translate] Terminology relating to medical polymer products Obsolete YY/T 1119-1999

PDF similar to YY/T 1119-2008


Standard similar to YY/T 1119-2008

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Basic data

Standard ID YY/T 1119-2008 (YY/T1119-2008)
Description (Translated English) Terminology relating to medical polymer products
Sector / Industry Medical Device & Pharmaceutical Industry Standard (Recommended)
Classification of Chinese Standard C48
Classification of International Standard 01.040.11
Word Count Estimation 22,215
Date of Issue 2008-10-17
Date of Implementation 2010-01-01
Older Standard (superseded by this standard) YY/T 1119-1999
Regulation (derived from) SFDA [2008] No. 605
Issuing agency(ies) State Food and Drug Administration
Summary This standard specifies the use of medical polymer materials, and direct or indirect contact with the body of the Medical Polymer terminology. This standard does not include artificial organs terminology. Note: This standard main collection contains national standards and pharmaceutical industry standards related terms appear, given the definition of the term applies only to medical polymer products and parts thereof, products or components used to guide the naming.

YY/T 1119-2008: Terminology relating to medical polymer products

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Terminology relating to medical polymer products ICS 01.040.11 C48 People's Republic of China pharmaceutical industry standards Replacing YY/T 1119-1999 Medical Polymer term Posted 2008-10-17 2010-01-01 implementation State Food and Drug Administration issued

Foreword

Instead of the standard YY/T 1119-1999 "Medical Polymer term." Compared with the standard YY/T 1119-1999 The main changes are as follows. The original version of the standard basis, the term was supplemented, and each chapter has been re-arranged. The standard medical infusion by the National Standardization Technical Committee appliances. This standard by the State Food and Drug Administration Jinan Medical Device Quality Supervision and Inspection Center. This standard was drafted. Shandong Medical Devices Product Quality Inspection Center. The main drafters of this standard. Wu Ping by Shaohua. This standard was first released in 1989 (ZBC48005-1989), 1999 first published revised edition (YY/T 1119-1999). Medical Polymer term

1 Scope

This standard specifies the use made of medical polymer materials and polymer products for medical term direct or indirect contact with the human body. This standard The term does not include artificial organs. Note. This standard mainly reproduces the relevant national standards and terms that appear in the pharmaceutical industry standard, the definition given to the term applies only to medical polymer products and Its means for guiding the product or component name.

2 Basic terms

2.1 By puncture or incision to insert the hose body. 2.2 Do not insert the hose human tissue. 2.3 Mucous membrane contact with the body or inserted intestine, esophagus, respiratory or other parts of the hose, the input liquid, gas and liquid nutrition into the body through which the Or body fluid from the body. NOTE. In many applications, the cannula is also known as a catheter. 2.4 X-ray opaque component For determining the position of the body on the medical polymer instrument X-ray opaque components for X-ray monitor. 2.5 Injection member The injectable medication to the body through it and having a resilient self-sealing of the puncture means. 2.6 It can collect seat (elastic means puncture self-sealing) or the valve body through a fluid sample from it. 2.7 Pipeline by fluid conduit principles or special equipment to make general closing or opening the device. 2.8 Pipeline only in one direction so that the liquid flow valve. 2.9 Release valve releasingvalve It requires the use of special equipment or a specified instrument (syringe) from the system to charge or release valve.

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