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Panoscreen I and II

FDA UDI

by Immucor, Inc.

Identity

Trade Name
Panoscreen I and II FDA UDI
Generic Name
Antibody screening reagent red blood cell IVD, kit, agglutination FDA UDI
Device Name
Panoscreen I and II is intended for use in the detection of unexpected IgG antibodies to red blood cells by manual tube method. The configuration of this product is a 2-cell screen. FDA UDI
Model / Reference
0002380 FDA UDI
Description
Panoscreen I and II is intended for use in the detection of unexpected IgG antibodies to red blood cells by manual tube method. The configuration of this product is a 2-cell screen. FDA UDI

Identifiers

Catalog Number
0002380 FDA UDI
Primary DI / UDI-DI
10888234000297 FDA UDI
GMDN Term
Antibody screening reagent red blood cell IVD, kit, agglutination FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

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

Category: Antibody screening reagent red blood cell IVD, kit, agglutination

Panoscreen I and II by Immucor, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antibody screening reagent red blood cell IVD, kit, agglutination.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Immucor, Inc.

Sources (1)

  • FDA UDI 5108ef5b-5649-40b6-ac96-cb31ca1ae343 35 fields · synced May 30, 2026