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Amico Diagnostic Otoscope DH-W35-OH

by Amico Diagnostic Incorporated

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 Number00697077003111 UDI-DI Date8 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  • Withdrawn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
Amico Diagnostic Otoscope
Generic Name
Otoscope, direct
Model / Reference
DH-W35-OH
Primary DI / UDI-DI
00697077003111
FDA Product Code
ERA
GMDN Term
Otoscope, direct
Device Class
Class I
Regulation Number
874.4770
GUDID distribution status
In Commercial Distribution

Other devices from Amico Diagnostic Incorporated

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Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

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