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Disposable Bite Block FTL-BB-AI-W

by Yangzhou Fartley Medical Instrument Technology Co., Ltd

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 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06936603235164 UDI-DI Date22 Oct 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  • Withdrawn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
Disposable Bite Block
Generic Name
Endoscopic bite block, basic, single-use
Model / Ref / Catalog
FTL-BB-AI-W, MP-05-30-30-T
Primary DI / UDI-DI
06936603235164
FDA Product Code
MNK
GMDN Term
Endoscopic bite block, basic, single-use
Device Class
Class I
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution

Other devices from Yangzhou Fartley Medical Instrument Technology Co., Ltd

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Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

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