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preclinical evaluation medical devices test methods selevtion scopethis standard test items evaluation articles chinastandards.net sodium indigo disulfonate neutron-gamma ray detection performance
YY/T 0268-2001 in English

YY/T 0268-2001 in English

SUPERSEDED

Dentistry--Preclinical evaluation of biocompatibility of medical devices used in dentistry--Part 1:Evaluation and test methods selevtion

  • Issued on:2001-11-09
  • Implemented on:2002-03-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $210.00
$204.00
Standard No: YY/T 0268-2001
Document status: SUPERSEDED
Superseded by: YY/T 0268-2008 Dentistry - Biological evaluation of medical devices used in dentistry Part1: Evaluation and test
Superseded on: 2009-12-01
Title in English: Dentistry--Preclinical evaluation of biocompatibility of medical devices used in dentistry--Part 1:Evaluation and test methods selevtion
Title in Chinese: 牙科学 用于口腔的医疗器械生物相容性临床前评价 第1单:评价与试验项目选择
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 1~3 business days
Issued on: 2001-11-09
Implemented on: 2002-03-01
Superseding: YY 0268-1995 Biological evaluation of dental materials --Unit 1:Guideline of biological evaluation of dental materials
Chinese Classification: C33-Stomatologic device, equipment and material
Professional Classification: YY-Pharmaceutics
Related Keywords: preclinical evaluation
medical devices
test methods selevtion scopethis standard
test items
evaluation
Related Topics: Non-clinical evaluation of medical devices,
Clinical Evaluation of Medical Devices
Biology Triple Evaluation
currently in clinical trials
Biocompatibility Evaluation
Biocompatibility Evaluation
Clinical Evaluation of Medical Devices
Dental medical device clinical trials
Clinical trial pre-test evaluation
Frontiers of Biological Sciences
Evaluation of non-clinical trials
Frontier Science Project
Frontiers in Biomedical Engineering
yy/t 0268
yy/t 0268-2008

本标准规定了用于口腔的医疗器械的分类及其生物相容性临床前评价与试验项目的选择。


Scope

This standard specifies the classification of medical devices used in the oral cavity and the selection of biocompatibility preclinical evaluation and test items.

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