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medical products

medical products, Total:54 items.

In the international standard classification, medical products involves: Medical equipment, Sterilization and disinfection, Applications of information technology, Technical product documentation, Medical sciences and health care facilities in general, Laboratory medicine, Pharmaceutics, Vocabularies.

Professional Standard - Medicine, medical products

• YY/T 0606.7-2008 Tissue engineered medical products.Part 7:Chitosan
• YY/T 0567.2-2005 Aseptic processing of health care products - Part 2: filtration
• YY/T 0606.3-2007 Tissue engineered medical products.Part 3:General classification
• YY/T 0606.8-2008 Tissue engineered medical products.Part 8:Alginate
• YY/T 0567.1-2005 Aseptic processing of health care products - Part 1: General requirements
• YY/T 0606.5-2007 Tissue engineered medical Products.Part 5:Characterization and testing of substrates and scaffolds
• YY/T 0606.4-2007 Tissue engineered medical product.Part 4:Terminology and classification of skin substitute
• YY/T 0606.12-2007 Tissue engineered medical products.Part 12:Guide for processing cells,tissues,and organs
• YY/T 0606.14-2014 Tissue engineered medical products.Part 14:Standard practice for evaluation of immune responses of substrate and scaffolds products:ELISA tests
• YY/T 0606.9-2007 Tissue engineered meedical products.Part 9:Sodium hyaluronate
• YY/T 0606.10-2008 Tissue engineered medical product.Part 10: In vivo assessment of implantable devices intended torepair or regenerate articular cartilage
• YY/T 0606.25-2014 Tissue engineered medical product.Part 25: Quantification of remnant DNA in biological materials utilizing animal tissues and their derivatives: Fluorescence method

British Standards Institution (BSI), medical products

• DD ENV 12610-1998 Medical informatics. Medical product identification
• DD ENV 12610:1998 Medical informatics. Medical product identification
• PD ISO/TS 21560:2020 General requirements of tissue-engineered medical products

GOST, medical products

• GOST R 56429-2021 Medical devices. Clinical еvaluation
• GOST IEC 62304-2022 Medical devices. Software. Life cycle processes
• GOST ISO 14971-2021 Medical devices. Application of risk management to medical devices
• GOST R ISO 15223-1-2010 Medical devices. Symbols to be used with medical device labels, labeling and information to be supplied. Part 1. General requirements
• GOST R IEC 62366-1-2023 Medical devices. Part 1. Application of usabilityengineering to medical devices
• GOST R 59771-2021 Personalized medical devices. Key terms and definitions

IN-BIS, medical products

• IS 10150-1981 Guidelines for Sterilization of Medical Products

HU-MSZT, medical products

• MNOSZ 14678-1955 Stands for medical products (suspended)

RU-GOST R, medical products

• GOST R 15.013-1994 System of product development and launching into manufacture. Medical products
• GOST R 50325-2011 Medical products. Radiation sterilization. Dosimetric techniques

CZ-CSN, medical products

• CSN 85 5200-1988 Climatic tests election for medical products

SCC, medical products

• BS PD ISO/TS 21560:2020 General requirements of tissue-engineered medical products

International Organization for Standardization (ISO), medical products

• IEC/TR 62653:2012 Guidelines for the safe use of medical products in dialysis treatment
• IEC TR 62653:2012 Guidelines for the safe use of medical products in dialysis treatment
• IEC TR 62653:2012 Guidelines for the safe use of medical products in dialysis treatment

American Society for Testing and Materials (ASTM), medical products

• ASTM F2211-02 Standard Classification for Tissue Engineered Medical Products (TEMPs)
• ASTM F2211-13 Standard Classification for Tissue Engineered Medical Products (TEMPs)
• ASTM F2211-04 Standard Classification for Tissue Engineered Medical Products (TEMPs)
• ASTM F2211-13(2021) Standard Classification for Tissue-Engineered Medical Products (TEMPs)
• ASTM F2312-10 Standard Terminology Relating to Tissue Engineered Medical Products
• ASTM F2312-04 Standard Terminology Relating to Tissue Engineered Medical Products
• ASTM F2312-03 Standard Terminology Relating to Tissue Engineered Medical Products
• ASTM F2312-24 Standard Terminology Relating to Tissue Engineered Medical Products
• ASTM F2312-11(2020) Standard Terminology Relating to Tissue Engineered Medical Products
• ASTM F2312-11 Standard Terminology Relating to Tissue Engineered Medical Products
• ASTM F2386-04 Standard Guide for Preservation of Tissue Engineered Medical Products (TEMPs)

KR-KS, medical products

• KS P ISO TS 21560-2021 General requirements of tissue-engineered medical products

Korean Agency for Technology and Standards (KATS), medical products

• KS P ISO TS 21560:2021 General requirements of tissue-engineered medical products

American National Standards Institute （ANSI), medical products

• ANSI/AAMI ST25-1987 Guideline for Industrial Moist Heat Sterilization of Medical Products

GSO, medical products

• GSO ASTM F2211:2023 Standard Classification for Tissue-Engineered Medical Products (TEMPs)
• BH GSO ASTM F2211:2023 Standard Classification for Tissue-Engineered Medical Products (TEMPs)

German Institute for Standardization, medical products

• DIN VDE 0753-4:2009 Guideline for the safe use of medical products in dialysis treatment - Text in German and English
• DIN 58946-1:1987 Sterilization; steam sterilizers for medical products; terminology

國(guó)家食品藥品監(jiān)督管理局, medical products

• YY/T 0507.2-2005 Sterile processing of medical products Part 2: Filtration
• YY/T 0507.1-2005 Sterile processing of medical products Part 1: General requirements

BELST, medical products

• STB 1019-2000 Designing and setting of medical products in то manufacture

GOSTR, medical products

• GOST 30392-1995 Medical products. Dosimetric techniques for radiation sterilization

US-AAMI, medical products

• ANSI/AAMI/ISO TIR17665-3:2014 Sterilization of health care products - Moist heat - Guidance on the designation of a medical product to a product family and processing category for steam sterilization

Underwriters Laboratories (UL), medical products

• UL 2800-1-1-2022 STANDARD FOR SAFETY Risk Concerns for Interoperable Medical Products

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