Search-Cyte Pool 0.8% 213663

GUDID 07640137340391

Reagent Red Blood Cells for use in the detection of unexpected antibodies. For in vitro diagnotic use.

Medion Grifols Diagnostics AG

Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen Pooled antibody screening reagent red blood cell IVD, antigen
Primary Device ID07640137340391
NIH Device Record Key9918b5ee-2448-41a6-a4d1-992c805362b4
Commercial Distribution StatusIn Commercial Distribution
Brand NameSearch-Cyte Pool 0.8%
Version Model Number1x10 ml
Catalog Number213663
Company DUNS483287020
Company NameMedion Grifols Diagnostics AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latextrue
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107640137340391 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-01-27

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