Your cart is currently empty!
“ISO 29701:2010 Nanotechnologies – Endotoxin test on nanomaterial samples for in vitro systems – Limulus amebocyte lysate (LAL) test” has been added to your cart. View cart
ISO 13079:2011
ISO 13079:2011 Laboratory glass and plastics ware – Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren method
CDN $173.00
Description
ISO 13079:2011 specifies requirements for single-use and re-usable glass and plastics tubes for measuring the erythrocyte sedimentation rate (ESR) by the Westergren method, and for a support to hold tubes during the performance of the test. These so-called “Westergren tubes” are also sometimes designated as “Westergren pipettes”. A procedure for measuring the erythrocyte sedimentation rate by the Westergren method is given in an informative annex.
ISO 13079:2011 does not apply to single-use containers for human venous blood specimen collection and their accessories for which other standards apply. It also does not apply for devices where the Westergren method has been used as basis to develop other, similar methods or equipment for the erythrocyte sedimentation rate determination.
Edition
1
Published Date
2011-07-06
Status
PUBLISHED
Pages
15
Language
English
Format
Secure PDF
Secure – PDF details
- Save your file locally or view it via a web viewer
- Viewing permissions are restricted exclusively to the purchaser
- Device limits - 3
- Printing – Enabled only to print (1) copy
See more about our Environmental Commitment
Abstract
ISO 13079:2011 specifies requirements for single-use and re-usable glass and plastics tubes for measuring the erythrocyte sedimentation rate (ESR) by the Westergren method, and for a support to hold tubes during the performance of the test. These so-called "Westergren tubes" are also sometimes designated as "Westergren pipettes". A procedure for measuring the erythrocyte sedimentation rate by the Westergren method is given in an informative annex.
ISO 13079:2011 does not apply to single-use containers for human venous blood specimen collection and their accessories for which other standards apply. It also does not apply for devices where the Westergren method has been used as basis to develop other, similar methods or equipment for the erythrocyte sedimentation rate determination.
Previous Editions
Can’t find what you are looking for?
Please contact us at:
Related Documents
-
ISO 17511:2020 In vitro diagnostic medical devices – Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
CDN $351.00 Add to cart -
ISO 20916:2019 In vitro diagnostic medical devices – Clinical performance studies using specimens from human subjects – Good study practice
CDN $351.00 Add to cart -
ISO 18113:2022 In vitro diagnostic medical devices – Information supplied by the manufacturer (labelling) – Part 2: In vitro diagnostic reagents for professional use
CDN $115.00 Add to cart -
ISO 16766:2024 Manufacturers’ considerations for in vitro diagnostic medical devices in a public health emergency
CDN $173.00 Add to cart
