Medical sterile jar
Medical sterile jar, Total:119 items.
The international standard classification for "Medical sterile jar" includes: Vessels and containers mounted on vehicles , Fruits. Vegetables , Medical materials , Sterilization and disinfection in general , Food microbiology , food products in general , Laboratory medicine .
The Chinese standard classification for "Medical sterile jar" includes: Other light industry machinery , Other canned foods , Medical sanitary products , Public medical equipment , Medical apparatus and devices in general , Food sanitation .
Professional Standard - Light Industry
- QB/T 4706-2014 Canned Dressing Edible Fungi
- QB/T 4110-2010 Sanitary stainless steel tank for storage and transport
Group Standards of the People's Republic of China
- T/CSBME 012-2019 Disposable sterile medical gauze blocks
- T/CSBME 014-2019 Disposable Sterile Medical Cotton Ball
- T/CAMDI 056-2020 Ethylene oxide sterilization process practice of sterile medical device
- T/CSBME 013-2019 Disposable sterile medical cotton stick
- T/CSBME 011-2019 Disposable use of sterile infusion tape
- T/CSBME 015-2019 Disposable sterile medical cap
- T/CSBME 010-2019 Disposable use of sterile medical pad/patic
Professional Standard - Medicine
- YY/T 0615.1-2007 Requirements for medical devices to be designated STERILE - Part 1: Requirements for terminally sterilized medical devices
- YY/T 0567.1-2013 Aseptic processing of health care products - Part 1: General requirements
- YY/T 0567.1-2005 Aseptic processing of health care products-
- YY/T 0615.2-2007 Requirements for medical devices to be designated“STERILE” - Part 2: Requirements for aseptically processed medical devices
- YY/T 0567.5-2011 Aseptic processing of health care products—Part 5:Sterilization in place
- YY 0033-2000 Good manufacture practice for sterile medical devices
- YY/T 0033-2000 Good manufacture practice for sterile medical devices
Professional Standard - Commodity Inspection
- SN/T 2100-2008 Commercial sterilization of canned food for rapid detection method
General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China
- GB/T 14151-2022 General quality requirements for canned edible fungi
- GB/T 19973.2-2005 Sterilization of medical devices -- Microbiological methods -- Part 2: Test of sterility performed in the validation of a sterilization process
- GB 7098-2003 Hygienic STANDARD for canned edible fungi
- GB 7098-1996 Hygienic standard for canned edible fungi
国家医药管理局
- YY/T 0033-1990 Good manufacture practice for sterile medical devices
国家食品药品监督管理局
- YY/T 0507.1-2005 Sterile processing of medical products Part 1: General requirements
国家药监局
- YY/T 0567.2-2021 Aseptic processing of health care products-Part 2:Sterilizing filtration
RU-GOST R
- GOST 28085-2013 Medicine remedies biological for veterinary use. Method of bacteriological control of sterility
- GOST R 54666-2011 Canned milk. Sterilized condensed milk. Specifications
- GOST 32742-2014 Semifinished products. Aseptically canned fruit and vegetable puree. Specifications
- GOST 33612-2015 Sterilized meat cans. Rendered lard with ingredients. Specifications
- GOST ISO 11607-2011 Packaging for terminally sterilized medical devices. General requirements
American National Standards Institute (ANSI)
- ANSI/ADA 102-1998 Non-Sterile Nitrile Gloves for Dentistry
- ANSI/ADA 103-2001 Non-Sterile Polyvinyl Chloride Gloves for Dentistry
- ANSI/AAMI ST79/A 3.2-2012 Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ANSI/AAMI ST79/A 3.6-2012 Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ANSI/AAMI ST79/A 3.7-2012 Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ANSI/AAMI ST79/A 3.4-2012 Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ANSI/AAMI ST79/A 3.3-2012 Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ANSI/AAMI ST79/A 3.1-2012 Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ANSI/AAMI ST79/A 3.5-2012 Comprehensive guide to steam sterilization and sterility assurance in health care facilities
SCC
- CAN/CGSB 20.27-M91-1991 Sterile or non-sterile, single-use medical examination gloves
- CAN/CGSB-20.27-M91-1991 Sterile or Non-Sterile Medical Examination Gloves for Single Use
- DIN 58953-8:2019 Sterilization - Sterile supply - Part 8: Logistics of sterile medical devices
- DIN EN 556-2 E:2014 Draft Document - Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE'' - Part 2: Requirements for aseptically processed medical devices; German version prEN 556-2:2014
- AENOR UNE-EN 556-2:2016 Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices
- DANSK DS/EN 556-2:2015 Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices
- AS 2385:1980 Single-use (sterile infusion sets for general medical use
- DIN 58953-8 E:2018 Draft Document - Sterilization - Sterile supply - Part 8: Logistics of sterile medical devices
- NS-EN 13824:2004 Sterilization of medical devices — Aseptic processing of liquid medical devices — Requirements
- UNE-EN 556-2:2004 Sterilization of medical devices - Requirements for medical devices to be designated STERILE - Part 2: Requirements for aseptically processed medical devices
- AS 1094:1981 Single-use syringes (sterile) for general medical use
- UNE-EN 13824:2005 Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
- NS-EN 556:1994 Sterilization of medical devices — Requirements for medical devices to be labelled "Sterile"
- AS 1094:1993 Medical equipment - Single-use syringes (sterile) for general medical use
- AAMI ST46-2002 Steam sterilization and sterility assurance in health care facilities
- AS 2696:1989 Medical equipment - Single-use urethral catheters (sterile) for general medical use
- AS 1094:1971 Single-use syringes (sterile) for general medical use
- AS 2696:1984 Medical equipment - Single-use urethral catheters (sterile) for general medical use
- AS T39:1969 Single-use syringes (sterile) for general medical use
- NS-EN 556-1:2001 Sterilization of medical devices — Requirements for medical devices to be designated "STERILE" — Part 1: Requirements for terminally sterilized medical devices
- NS-EN 556-1:2024 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices
- AS 1946:1976 Single-use hypodermic needles (sterile) for general medical use
- DANSK DS/EN 556-1:2001 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices
- AAMI ST79:2006 Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- NS-EN 556:1994+A1:1998 Sterilization of medical devices — Requirements for terminally-sterilized medical devices to be labelled "Sterile" (including amendment A1:1998)
- BS EN 556:1995 Sterilization of medical devices. Requirements for terminally-sterilized devices to be labelled 'Sterile'
- AS T48:1970 Single-use hypodermic needles (sterile) for general medical use
- AENOR UNE-EN 556-1:2002 Sterilization of medical products. Requirements for medical devices to be designated "STERILE". Part 1: Requirements for sterilized medical devices in their terminal state.
- BS EN ISO 11737-2:2000 Sterilization of medical devices. Microbiological methods-Tests of sterility performed in the validation of a sterilization process
- DANSK DS/ISO/TS 22421:2021 Sterilization of health care products – Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
- NS-EN 556-2:2015 Sterilization of medical devices — Requirements for medical devices to be designated "STERILE" — Part 2: Requirements for aseptically processed medical devices
British Standards Institution (BSI)
- BS EN 556-2:2004 Sterilization of medical devices. Requirements for medical devices to be designated "STERILE". Requirements for aseptically processed medical devices
- BS EN 556-2:2015 Sterilization of medical devices. Requirements for medical devices to be designated 'STERILE'. Requirements for aseptically processed medical devices
- BS EN 13824:2004 Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
- BS EN 556-1:2024 Sterilization of medical devices. Requirements for medical devices to be designated "STERILE" - Requirements for terminally sterilized medical devices
- 23/30457240 DC BS EN 556-2. Sterilization of medical devices. Requirements for medical devices to be designated ''STERILE" - Part 2. requirements for aseptically processed medical devices
- BS EN 556-1:2001 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Requirements for terminally sterilized medical devices
- BS ISO 18746:2016 Traditional Chinese medicine. Sterile intradermal acupuncture needles for single use
- 23/30457243 DC BS EN 556-1. Sterilization of medical devices. Requirements for medical devices to be designated "STERILE" - Part 1. Requirements for terminally sterilized medical devices
- PD ISO/TS 22421:2021 Sterilization of health care products. Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
DIN
- DIN 58953-8:2003 Sterilization - Sterile supply - Part 8: Logistics of sterile medical devices
- DIN EN 13824:2005 Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
German Institute for Standardization
- DIN 58953-8:2019-03 Sterilization - Sterile supply - Part 8: Logistics of sterile medical devices
- DIN EN 556-1:2024 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices
- DIN EN 556-2:2023-02 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: requirements for aseptically processed medical devices; German and English version prEN 556-2:2023 / Note: Date of issue 2023-01-06*Intended as r...
- DIN EN 556-2:2015-11 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices; German version EN 556-2:2015 / Note: To be replaced by DIN EN 556-2 (2023-02).
ES-UNE
- UNE-EN 556-2:2016 Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices
- UNE-EN 556-1:2002/AC:2007 Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devices
Lithuanian Standards Office
- LST EN 556-2-2004 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices
- LST EN 556-1-2002/AC-2006 Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devices
Danish Standards Foundation
- DS/EN 556-2:2004 Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 2: Requirements for aseptically processed medical devices
- DS/EN 556-1/AC:2006 Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 1: Requirements for terminally sterilized medical devices
- DS/EN 556-1:2002 Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 1: Requirements for terminally sterilized medical devices
- DS/ISO/TS 22421:2021 Sterilization of health care products – Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
Standard Association of Australia (SAA)
- AS 2385:1990/Amdt 1:1993 Disposable (sterile) infusion set for general medical use
- ISO 6559:2024 Traditional Chinese medicine - Sterile three-edge needle for single use
Association Francaise de Normalisation
- NF S98-107-2*NF EN 556-2:2015 Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE'' - Part 2 : requirements for aseptically processed medical devices
- XP ISO/TS 22421:2021 Sterilization of healthcare products - Common requirements for sterilizers used for terminal sterilization of medical devices in healthcare settings
- XP S98-224*XP ISO/TS 22421:2021 Sterilization of health care products - Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
- NF S98-117:2005 Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements.
CEN - European Committee for Standardization
- EN 13824:2004 Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
European Committee for Standardization (CEN)
- EN 556:1994 Sterilization of Medical Devices - Requirements for Medical Devices to Be Labelled `Sterile'
- prEN 556-1991 Sterilization of medical devices; sterility assurance level for medical devices labelled "Sterile"; requirements
PT-IPQ
- NP EN 556-2000 Sterilization of medical devices Requirements for terminally sterilized medical devices to be labelled"Sterile"
ZA-SANS
- SANS 68:2003 Single-use sterile rubber surgical gloves - Specification
GSO
- GSO ASTM D7102:2021 Standard Guide for Determination of Endotoxin on Sterile Medical Gloves
- BH GSO ASTM D7102:2022 Standard Guide for Determination of Endotoxin on Sterile Medical Gloves
- GSO ISO/TS 22421:2023 Sterilization of health care products — Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
- BH GSO ISO/TS 22421:2023 Sterilization of health care products — Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
American Society for Testing and Materials (ASTM)
- ASTM D7102-17 Standard Guide for Determination of Endotoxin on Sterile Medical Gloves
- ASTM D7102-17(2022) Standard Guide for Determination of Endotoxin on Sterile Medical Gloves
- ASTM D7102-10 Standard Guide for Determination of Endotoxin on Sterile Medical Gloves
Indonesia Standards
- SNI 16-6642-2002 Medical equipment single use winged intravenous devices (sterile) for general medical use
- SNI 16-6654-2002 Single-use sterile infusion sets for general medical
International Organization for Standardization (ISO)
- ISO 11607:1997 Packaging for terminally sterilized medical devices
- ISO 11607:2003 Packaging for terminally sterilized medical devices
- ISO 18746:2016 Traditional Chinese medicine - Sterile intradermal acupuncture needles for single use
- ISO 13408-1:1998 Aseptic processing of health care products - Part 1: General requirements
NZ-SNZ
- AS/NZS 2485:1995 Medical Equipment - Single-Use Winged Intravenous Devices (Sterile) for General Medical Use
Korean Agency for Technology and Standards (KATS)
- KS P ISO 13408-1:2010 Aseptic processing of health care products-Part 1:General requirements
- KS P ISO 13408-1:2017 Aseptic processing of health care products-Part 1:General requirements