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Disposable Silicone Laryngeal Mask Airway La-77115

by Besmed Health Business Corp.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04716770771151 UDI-DI Date22 Jul 2019ListedStatusListed 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  • Withdrawn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 Silicone Laryngeal Mask Airway
Generic Name
Oropharyngeal airway, single-use
Model / Reference
LA-77115
Primary DI / UDI-DI
04716770771151
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 Besmed Health Business Corp.

See all devices from Besmed Health Business Corp. →

Properties

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

Other properties (6)

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