发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22
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本文件规定了压力蒸汽灭菌器、干热灭菌器(柜)、环氧乙烷灭菌器、低温蒸汽甲醛灭菌器、过氧化氢气体等离子体灭菌器灭菌效果鉴定试验的试验器材、试验步骤、评价规定以及注意事项。 本文件适用于压力蒸汽灭菌器、干热灭菌器(柜)、环氧乙烷灭菌器、低温蒸汽甲醛灭菌器、过氧化氢气体等离子体灭菌器灭菌效果的评价
Evaluating method for the efficacy of sterilization for disinfection equipment
The General Services Administration has authorized the use of this commercial item description in preference to A-A-O051382 (DM) dated 1 April 1986
STERILIZER, SURGICAL INSTRUMENT
The following National Stock Number is coveired by this document
CASE, BONE NAIL AND INSTRUMENT STERILIZATION
Sterilising Medical instruments Set
This Commercial Item Description covers an instrument suitable for holding ringed forceps during the sterilization process
HOLDER, SURGICAL INSTRUMENT STERILIZATION
This Commercial Item Description covers an instrument suitable for holding ringed forceps during sterilization
HOLDER, SURGICAL INSTRUMENT STERILIZATION
Sterilization of medical devices. Dry heat. Requirements for development, validation and routine control of a sterilization process for medical devices
The General Services Administration has authorized the use of this Commercial Item Description
RACK, INSTRUMENT STERILIZATION
Sterilisation of medical devices - Risk management related to the preparation of sterile medical devices within health establishments.
The General Services Administration has authorized the use of this Commercial Item Description
STERILIZER, SURGICAL INSTRUMENTS
This European Standard specifies the requirements for an aseptically processed medical deviceto be designated 'STERILE'.NOTE ForThe purpose
Sterilization of medical devices Requirements for medical devices to be designated STERILE Part 2: Requirements for aseptically processed medical devices
This European Standard specifies the requirements for an aseptically processed medical device to be designated 'STERILE'. NOTE For the purpose
"Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 2: Requirements for aseptically processed medical devices"
This Commercial Item Description covers a compartmented dental instrument case suitable for holding and autoclaving endodontic instruments
CASE, DENTAL INSTRUMENTS (STERILIZING AND STORAGE)
The General Services Administration has authorized the use of this Commercial Item Description as a replacement for Military Specification
STERILIZER, SURGICAL INSTRUMENT AND DRESSING
The General Services Administration has authorized the use of this Commercial Item Description as a replacement for MIL-S-36500A, which is cancelled
STERILIZER, SURGICAL INSTRUMENT AND DRESSING
本文件规定了压力蒸汽灭菌器、干热灭菌器(柜)、环氧乙烷灭菌器、低温蒸汽甲醛灭菌器、过氧化氢气体等离子体灭菌器灭菌效果鉴定试验的试验器材、试验步骤、评价规定以及注意事项。 本文件适用于压力蒸汽灭菌器、干热灭菌器(柜)、环氧乙烷灭菌器、低温蒸汽甲醛灭菌器、过氧化氢气体等离子体灭菌器灭菌效果的评价
Evaluating method for the efficacy of sterilization for disinfection equipment
The General Services Administration has authorized the use of this commercial item description in preference to A-A-O051382 (DM) dated 1 April 1986
STERILIZER, SURGICAL INSTRUMENT
The following National Stock Number is coveired by this document
CASE, BONE NAIL AND INSTRUMENT STERILIZATION
Sterilising Medical instruments Set
This Commercial Item Description covers an instrument suitable for holding ringed forceps during the sterilization process
HOLDER, SURGICAL INSTRUMENT STERILIZATION
This Commercial Item Description covers an instrument suitable for holding ringed forceps during sterilization
HOLDER, SURGICAL INSTRUMENT STERILIZATION
Sterilization of medical devices. Dry heat. Requirements for development, validation and routine control of a sterilization process for medical devices
The General Services Administration has authorized the use of this Commercial Item Description
RACK, INSTRUMENT STERILIZATION
Sterilisation of medical devices - Risk management related to the preparation of sterile medical devices within health establishments.
The General Services Administration has authorized the use of this Commercial Item Description
STERILIZER, SURGICAL INSTRUMENTS
This European Standard specifies the requirements for an aseptically processed medical deviceto be designated 'STERILE'.NOTE ForThe purpose
Sterilization of medical devices Requirements for medical devices to be designated STERILE Part 2: Requirements for aseptically processed medical devices
This European Standard specifies the requirements for an aseptically processed medical device to be designated 'STERILE'. NOTE For the purpose
"Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 2: Requirements for aseptically processed medical devices"
This Commercial Item Description covers a compartmented dental instrument case suitable for holding and autoclaving endodontic instruments
CASE, DENTAL INSTRUMENTS (STERILIZING AND STORAGE)
The General Services Administration has authorized the use of this Commercial Item Description as a replacement for Military Specification
STERILIZER, SURGICAL INSTRUMENT AND DRESSING
The General Services Administration has authorized the use of this Commercial Item Description as a replacement for MIL-S-36500A, which is cancelled
STERILIZER, SURGICAL INSTRUMENT AND DRESSING