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Capture-P Control set

FDA UDI

Class I (US FDA UDI)

by Immucor, Inc.

Identity

Trade Name
Capture-P Control set FDA UDI
Generic Name
Human platelet antigen (HPA) multiple antibody screening/identification IVD, kit, agglutination FDA UDI
Device Name
The Capture-P Control set is composed of both negative and weak positive control material to control both the Capture-P and Capture-P Ready-Screen tests. FDA UDI
Model / Reference
0066248 FDA UDI
Description
The Capture-P Control set is composed of both negative and weak positive control material to control both the Capture-P and Capture-P Ready-Screen tests. FDA UDI

Identifiers

Catalog Number
0066248 FDA UDI
Primary DI / UDI-DI
10888234001294 FDA UDI
FDA Product Code
KSS FDA UDI
GMDN Term
Human platelet antigen (HPA) multiple antibody screening/identification IVD, kit, agglutination FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.9050 FDA UDI
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

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

Category: Human platelet antigen (HPA) multiple antibody screening/identification IVD, kit, agglutination

Capture-P Control set by Immucor, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Human platelet antigen (HPA) multiple antibody screening/identification IVD, kit, agglutination.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Immucor, Inc.

Sources (1)

  • FDA UDI 973c2a1f-0a71-451c-ae91-801abb154274 37 fields · synced May 30, 2026