ISO 6717:2021 PDF

ISO 6717:2021 PDF

Name:
ISO 6717:2021 PDF

Published Date:
09/01/2021

Status:
Active

Description:

In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood

Publisher:
International Organization for Standardization

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Russian version):
200 business days

SKU:

Choose Document Language:
$37.2
Need Help?

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.


File Size : 1 file , 1.3 MB
Note : This product is unavailable in Ukraine, Russia, Belarus
Published : 09/01/2021
Same As : ISO 6717:2021

History


Related products

ISO 18113-2:2022
Published Date: 09/30/2022
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
$24.3
ISO 18113-3:2022
Published Date: 09/30/2022
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
$24.3
ISO 16256:2021
Published Date: 10/01/2021
Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
$37.2
ISO 20186-1:2019
Published Date: 03/01/2019
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA
$49.8

Best-Selling Products

CAN/CSA-ISO/IEC TR 10032-04 (R2019)
Published Date: 12/01/2004
Information Technology - Reference Model of Data Management (Adopted ISO/IEC TR 10032:2003, first edition, 2003-11-01)
$53.4
CAN/CSA-ISO/IEC TR 10176-04 (R2022)
Published Date: 01/01/2004
nformation Technology - Guidelines for the Preparation of Programming Language Standards (Adopted ISO/IEC TR 10176:2001, third edition, 2001-07-01)
$48
CAN/CSA-ISO/IEC TR 11179-2:20
Published Date: 03/01/2020
Information technology - Metadata registries (MDR) - Part 2: Classification (Adopted ISO/IEC TR 11179-2:2019, first edition, 2019-04)
$21
CAN/CSA-ISO/IEC TR 11801-9905:19
Published Date: 10/01/2019
Information technology - Generic cabling for customer premises - Part 9905: Guidelines for the use of installed cabling to support 25GBASE-T application (Adopted ISO/IEC TR 11801-9905:2018, first edition, 2018-02)
$45
CAN/CSA-ISO/IEC TR 11801-9906:20
Published Date: 11/01/2020
Information technology - Generic cabling for customer premises - Part 9906: Balanced 1-pair cabling channels up to 600 MHz for single pair Ethernet (SPE) (Adopted ISO/IEC TR 11801-9906:2020, first edition, 2020-02)
$55.5
CAN/CSA-ISO/IEC TR 11801-9907:20
Published Date: 07/01/2020
Information technology - Generic cabling for customer premises - Part 9907: Specifications for direct attach cabling (Adopted ISO/IEC TR 11801-9907:2019, first edition, 2019-07)
$30