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Echinococcus IgG ELISA EIA-3472

by DRG International, Inc.

Echinococcus IgG ELISA EIA-3472 is a Class I device made by DRG International, Inc., listed in FDA GUDID since 24 Aug 2023 (UDI-DI 00840239034724), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840239034724 UDI-DI Date24 Aug 2023ListedStatusListed 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  • Withdrawn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
Echinococcus IgG ELISA
Generic name
Echinococcus granulosus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Model / Ref / Catalog
EIA-3472
Primary DI / UDI-DI
00840239034724
FDA product code
GPF
GMDN term
Echinococcus granulosus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Device class
Class I
Regulation number
866.3200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Echinococcus granulosus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Other devices from DRG International, Inc.

See all devices from DRG International, Inc. →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)