CLSI GP39

Tubes and Additives for Venous and Capillary Blood Specimen Collection, 6th Edition

This standard contains requirements for the materials, manufacturing, and labeling of venous and capillary blood collection devices.

This document is available in electronic format only.

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Chairholder: Nancy Dubrowny, MS, MT(ASCP)SC

Date of Publication: December 29, 2010

Order Code PDF: CLSI GP39A6E
ISBN Number: 1-56238-740-5

Order Code Print: print not available

Edition: Sixth

Pages: 28

CLSI GP39 Additional Details

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The U.S. Food and Drug Administration (FDA) has evaluated and recognized this approved-level consensus standard for use in satisfying a regulatory requirement.

This document was formerly sold under the code H01-A6.

This archived document is no longer being reviewed through the CLSI Consensus Document Development Process. However, this document is technically valid as of August 2021. Because of its value to the laboratory community, it is being retained in CLSI’s library.

CLSI GP39 Abstract

Clinical and Laboratory Standards Institute document GP39-A6—Tubes and Additives for Venous and Capillary Blood Specimen Collection; Approved Standard—Sixth Edition is a performance standard for manufacturers of venous and capillary blood collection tubes and additives for serum, plasma, and whole blood testing. GP39 addresses requirements for the materials, construction, and labeling of venous and capillary blood collection tubes and tube assemblies.