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Anti-Adenovirus IFA (IgG) FI 2680-1010 G

by EUROIMMUN Medizinische Labordiagnostika AG

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04049016059400 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Anti-Adenovirus IFA (IgG)
Generic Name
Adenovirus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay
Model / Reference
FI 2680-1010 G
Primary DI / UDI-DI
04049016059400
FDA Product Code
GNY
GMDN Term
Adenovirus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay
Device Class
Class I
Regulation Number
866.3020
GUDID distribution status
Not in Commercial Distribution

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Properties

  • Single Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

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