BKMAM

GUDID 16976018090016

Changde BKMAM Biotechnology Co.,Ltd.

Centrifuge tube IVD
Primary Device ID16976018090016
NIH Device Record Key9d087636-e757-4b63-8af7-65ce71d246a4
Commercial Distribution StatusIn Commercial Distribution
Brand NameBKMAM
Version Model Number50ml
Company DUNS553252351
Company NameChangde BKMAM Biotechnology Co.,Ltd.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS116976018090016 [Primary]

FDA Product Code

FMHContainer, Specimen, Sterile

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-05
Device Publish Date2023-03-28

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.