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AccuDiag™ Human Growth Hormone (HGH) ELISA DACD1901-15

by Diagnostic Automation, 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850049545815 UDI-DI Date27 Jan 2026ListedStatusListed 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  • Withdrawn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
AccuDiag™ Human Growth Hormone (HGH) ELISA
Generic Name
Human growth hormone (HGH) IVD, kit, enzyme immunoassay (EIA)
Model / Ref / Catalog
DACD1901-15, 1901-15
Primary DI / UDI-DI
00850049545815
FDA Product Code
CFL
GMDN Term
Human growth hormone (HGH) IVD, kit, enzyme immunoassay (EIA)
Device Class
Class I
Regulation Number
862.1370
GUDID distribution status
In Commercial Distribution

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Properties

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

Other properties (10)

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