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Beckman Coulter® PK® Systems Anti-E (906)

FDA UDI

by Diagast

Identity

Trade Name
Beckman Coulter® PK® Systems Anti-E (906) FDA UDI
Generic Name
Anti-E [RH003] red blood cell grouping IVD, antibody FDA UDI
Device Name
Blood Grouping Reagent Anti-E (Monoclonal) formulated for Automated Systems, Beckman Coulter® PK® Systems FDA UDI
Model / Reference
17307 FDA UDI
Description
Blood Grouping Reagent Anti-E (Monoclonal) formulated for Automated Systems, Beckman Coulter® PK® Systems FDA UDI

Identifiers

Catalog Number
17307 FDA UDI
Primary DI / UDI-DI
23661562173079 FDA UDI
GMDN Term
Anti-E [RH003] red blood cell grouping IVD, antibody FDA UDI

Classification

Commercial Distribution
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

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anti-E [RH003] red blood cell grouping IVD, antibody

Beckman Coulter® PK® Systems Anti-E (906) by Diagast — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anti-E [RH003] red blood cell grouping IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diagast

Sources (1)

  • FDA UDI 8d32d1d9-d9ce-441c-a190-8de271a3206e 36 fields · synced Jun 6, 2026