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AutoSink Adapter, Fuji Duodenoscope with ERCP T9-ADPT-2F

by Torvan Medical 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 Number00816185001202 UDI-DI Date19 Jun 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  • Withdrawn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
AutoSink Adapter, Fuji Duodenoscope with ERCP
Generic Name
Invasive medical device leak tester, electrical
Model / Ref / Catalog
T9-ADPT-2F
Primary DI / UDI-DI
00816185001202
FDA Product Code
FCY
GMDN Term
Invasive medical device leak tester, electrical
Device Class
Class I
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution

Other devices from Torvan Medical Inc

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Properties

  • Premarket Exempt
  • Serial Number

Other properties (12)

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