Pak12®G - Pak12G assay is a qualitative solid phase enzyme - IMMUCOR GTI DIAGNOSTICS, INC.

Duns Number:606034197

Device Description: Pak12G assay is a qualitative solid phase enzyme linked immunosorbent assay (ELISA) design Pak12G assay is a qualitative solid phase enzyme linked immunosorbent assay (ELISA) designed to detect IgG antibodies to HLA class I antigens and to epitopes on the platelet glycoproteins IIb/IIIa, Ia/IIa, and Ib/IX.

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More Product Details

Catalog Number

PAK12G

Brand Name

Pak12®G

Version/Model Number

PAK12G

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 15, 2017

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

BK930032,BK950004

Product Code Details

Product Code

MYP

Product Code Name

Test,Platelet Antibody

Device Record Status

Public Device Record Key

2af275b3-8aab-4bab-a67a-1f95570ad152

Public Version Date

August 01, 2018

Public Version Number

4

DI Record Publish Date

July 08, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"IMMUCOR GTI DIAGNOSTICS, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 54
U Unclassified 36