This European Standard specifies the requirements for a terminally-sterilized medical device to bedesignated “STERILE”. Part 2 of this European Standard specifies the requirements for an asepticallyprocessed medical...
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标准号:
BS EN 556-1-2001
This European Standard specifies the requirements for a terminally-sterilized medical device to bedesignated “STERILE”. Part 2 of this European Standard specifies the requirements for an asepticallyprocessed medical device to be designated “STERILE”.
The document specifies requirements for sterile single-use hypodermic syringes made of plastic materials and intended for the aspiration of fluids of for the injection of fluids immediately after filling.
标准号:
DIN EN ISO 7886-1-1997
The document specifies requirements for sterile single-use hypodermic syringes made of plastic materials and intended for the aspiration of fluids of for the injection of fluids immediately after filling.
This part of ISO 10555 specifies requirements for cen-tral venous catheters supplied in the sterile condition, and intended for single use. NOTE 1 Attention is drawn to ISO 11070, which specifies requirements for acce...
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标准号:
BS EN ISO 10555-3-1997
This part of ISO 10555 specifies requirements for cen-tral venous catheters supplied in the sterile condition, and intended for single use. NOTE 1 Attention is drawn to ISO 11070, which specifies requirements for accessory devices for use with intra-vascular catheters.
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