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NA Oropharyngeal airway(Model:10.0#)

by Henan Tuoren Medical Device 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06938119388266 UDI-DI Date19 Nov 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Oropharyngeal airway, single-use
Model / Reference
Oropharyngeal airway(Model:10.0#)
Primary DI / UDI-DI
06938119388266
FDA Product Code
CAE
GMDN Term
Oropharyngeal airway, single-use
Device Class
Class I
Regulation Number
868.5110
GUDID distribution status
In Commercial Distribution

Related devices

Category: Oropharyngeal airway, single-use

Other devices from Henan Tuoren Medical Device Co., Ltd.

See all devices from Henan Tuoren Medical Device Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No