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Solidscreen II Strip

FDA UDI

Class II (US FDA UDI)

by Bio-Rad Medical Diagnostics GmbH

Identity

Trade Name
Solidscreen II Strip FDA UDI
Generic Name
Solid-phase red blood cell adherence antibody/antigen IVD FDA UDI
Device Name
Microplate for use in detection of red blood cell antibodies and antigens in indirect and direct antiglobulin tests with solid phase antiglobulin technique on TANGO instruments; 10 plates FDA UDI
Model / Reference
806521100 FDA UDI
Description
Microplate for use in detection of red blood cell antibodies and antigens in indirect and direct antiglobulin tests with solid phase antiglobulin technique on TANGO instruments; 10 plates FDA UDI

Identifiers

Catalog Number
806521100 FDA UDI
Primary DI / UDI-DI
07611969951499 FDA UDI
FDA Product Code
KSZ FDA UDI
GMDN Term
Solid-phase red blood cell adherence antibody/antigen IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9175 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

Yes

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: Solid-phase red blood cell adherence antibody/antigen IVD

Solidscreen II Strip by Bio-Rad Medical Diagnostics GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Solid-phase red blood cell adherence antibody/antigen IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e869601-a3f5-4b17-9f0f-8bf5949f0792 37 fields · synced Jun 8, 2026