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Database: 365,228(8 Aug 2026)

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

Group Standards of the People's Republic of China

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)

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)

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)