← Back to catalogue

Biotestcell® 3

FDA UDI

by Bio-Rad Medical Diagnostics GmbH

Identity

Trade Name
Biotestcell® 3 FDA UDI
Generic Name
Antibody screening reagent red blood cell IVD, kit, agglutination FDA UDI
Device Name
Reagent Red Blood Cells; 3.0 - 3.4%; for use in detection of unexpected antibodies with TANGO instruments and by tube test; 3x10ml FDA UDI
Model / Reference
816085100 FDA UDI
Description
Reagent Red Blood Cells; 3.0 - 3.4%; for use in detection of unexpected antibodies with TANGO instruments and by tube test; 3x10ml FDA UDI

Identifiers

Catalog Number
816085100 FDA UDI
Primary DI / UDI-DI
07611969952687 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

Biotestcell® 3 by Bio-Rad Medical Diagnostics GmbH — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI fd27ed8a-d782-4e77-9282-1afcedb9e8c4 35 fields · synced Jun 6, 2026