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UniMatch™ Plus Software 790111

by One Lambda, Inc.

UniMatch Plus Software 790111 is a HLA class I & II antigen tissue typing IVD (FDA unclassified; FDA product code MZI, Test,Qualitative,For Hla,Non-Diagnostic) made by One Lambda, Inc., listed in FDA GUDID since 31 Aug 2016 (UDI-DI 00814695022496), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00814695022496 UDI-DI Date31 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
UniMatch™ Plus Software
Generic name
HLA class I & II antigen tissue typing IVD, kit, multiplex
Catalogue number
790111
Primary DI / UDI-DI
00814695022496
FDA product code
MZI
GMDN term
HLA class I & II antigen tissue typing IVD, kit, multiplex
Device class
U
GUDID distribution status
In Commercial Distribution

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Properties

  • Prescription use
  • Convenience kit
  • Serial number
Other properties (12, all answered No)