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Product | ISO 6717:2021 | ||
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Price | Price USD 106.00 | ||
Rating | Rating | ||
Buy | Buy Add to Cart | ||
Description |
Description
This document specifies requirements and test methods for specialized single-use evacuated and non-evacuated containers, intended by their manufacturers, for the primary containment and preservation of specimens, other than blood specimens, derived from the human body, for the purposes of in vitro diagnostic examination. It is not intended to cover specimen containers for forensic investigations. Examples of such specimens include, but are not limited to, cerebral spinal fluid (CSF), faeces, infected bodily fluids, saliva, ejaculate, sputum, urine, tissue samples. Specimens and types of devices specifically excluded are specialized containers for cryo-preservation, samples for nucleic acid testing and swabs. NOTE Requirements and test methods for evacuated and non-evacuated single-use human venous blood specimen collection containers are specified in ISO 6710. This document does not specify requirements for auxiliary devices used in conjunction with specimen containers. |
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Standard Number | Standard Number ISO 6717:2021 | ||
Title | Title ISO 6717:2021 In vitro diagnostic medical devices — Single-use containers for the collection of specimens from humans other than blood | ||
Status | Status Published | ||
Publication Date | Publication Date 26 Aug 2021 | ||
Cross References | Cross References | ||
Descriptors | Descriptors | ||
ICS | ICS 11.100.10 | ||
Committee | Committee ISO/TC 76 Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use | ||
ISBN | ISBN | ||
Publisher | Publisher PECB Store | ||
Format | Format PDF | ||
Delivery | Delivery NO | ||
Pages | Pages 14 | ||
File Size | File Size KB |