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Positive Control Serum

FDA UDI

Class U (US FDA UDI)

by Immucor GTI Diagnostics, Inc.

Identity

Trade Name
Positive Control Serum FDA UDI
Generic Name
HLA class II antigen tissue typing IVD, kit, multiplex FDA UDI
Device Name
For Use with LIFECODES Class II IDv2 FDA UDI
Model / Reference
403892 FDA UDI
Description
For Use with LIFECODES Class II IDv2 FDA UDI

Identifiers

Catalog Number
403892 FDA UDI
Primary DI / UDI-DI
10888234400615 FDA UDI
FDA Product Code
MZI FDA UDI
GMDN Term
HLA class II antigen tissue typing IVD, kit, multiplex FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Positive Control Serum by Immucor GTI Diagnostics, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2399e1fe-d42e-4b9f-96d9-4e55311270a9 38 fields · synced May 30, 2026