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Erytype S RhD Confirm

FDA UDI

by Bio-Rad Medical Diagnostics GmbH

Identity

Trade Name
Erytype S RhD Confirm FDA UDI
Generic Name
Rhesus (Rh) phenotype (CcDEe)/Kell phenotype multiple blood grouping IVD, kit, agglutination FDA UDI
Device Name
Microplate for the detection of the D antigen on human red blood cells with TANGO instruments, 10 Plates FDA UDI
Model / Reference
806190100 FDA UDI
Description
Microplate for the detection of the D antigen on human red blood cells with TANGO instruments, 10 Plates FDA UDI

Identifiers

Catalog Number
806190100 FDA UDI
Primary DI / UDI-DI
07611969965687 FDA UDI
GMDN Term
Rhesus (Rh) phenotype (CcDEe)/Kell phenotype multiple blood grouping 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

No

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: Rhesus (Rh) phenotype (CcDEe)/Kell phenotype multiple blood grouping IVD, kit, agglutination

Erytype S RhD Confirm by Bio-Rad Medical Diagnostics GmbH — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rhesus (Rh) phenotype (CcDEe)/Kell phenotype multiple blood grouping IVD, kit, agglutination.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio-Rad Medical Diagnostics GmbH

Sources (1)

  • FDA UDI 5908f800-8c5b-4d3f-ba1f-7c92931fd184 35 fields · synced Jun 6, 2026