Gt F(ab')2 Anti-Human IgA (a) FITC Conjugate

GUDID 10190302009041

LIFE TECHNOLOGIES CORPORATION

Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent Multiple CD cell marker IVD, reagent
Primary Device ID10190302009041
NIH Device Record Keyd7cc20bb-aba1-45e2-870d-42dbb8c990bc
Commercial Distribution StatusIn Commercial Distribution
Brand NameGt F(ab')2 Anti-Human IgA (a) FITC Conjugate
Version Model NumberH14101
Company DUNS080131636
Company NameLIFE TECHNOLOGIES CORPORATION
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110190302009041 [Primary]

FDA Product Code

MVUREAGENTS,SPECIFIC,ANALYTE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2020-03-19
Device Publish Date2018-03-07