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Glomerular Basement Membrane (Primate Kidney) 5648L

by Zeus Scientific, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00845533002028 UDI-DI Date17 Oct 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Glomerular Basement Membrane (Primate Kidney)
Generic Name
Glomerular basement membrane antibody (Goodpasture antibody) IVD, kit, fluorescent immunoassay
Model / Ref / Catalog
5648L
Primary DI / UDI-DI
00845533002028
FDA Product Code
MVJ
GMDN Term
Glomerular basement membrane antibody (Goodpasture antibody) IVD, kit, fluorescent immunoassay
Device Class
Class II
Regulation Number
866.5660
GUDID distribution status
In Commercial Distribution

Other devices from Zeus Scientific, Inc.

See all devices from Zeus Scientific, Inc. →

Properties

  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No