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FlowPRA™ HLA Class I Screening Test

FDA UDI

by One Lambda, Inc.

Identity

Trade Name
FlowPRA™ HLA Class I Screening Test FDA UDI
Generic Name
HLA class I & II antibody screening IVD, kit, multiplex FDA UDI
Device Name
The FlowPRA Screening Test is intended for use in flow cytometric detection of panel reactive antibody (PRA) against pooled HLA Class I or Class II antigens. FDA UDI
Model / Reference
N/A FDA UDI
Description
The FlowPRA Screening Test is intended for use in flow cytometric detection of panel reactive antibody (PRA) against pooled HLA Class I or Class II antigens. FDA UDI

Identifiers

Catalog Number
FL1-30 FDA UDI
Primary DI / UDI-DI
00812117011288 FDA UDI
GMDN Term
HLA class I & II antibody screening IVD, kit, multiplex 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

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

Yes

FDA UDI

Category: HLA class I & II antibody screening IVD, kit, multiplex

FlowPRA™ HLA Class I Screening Test by One Lambda, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as HLA class I & II antibody screening IVD, kit, multiplex.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
One Lambda, Inc.

Sources (1)

  • FDA UDI fb759fa3-b7eb-42fd-964d-5c7b1dff36ed 36 fields · synced May 30, 2026