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SourceMark M0371

by Sourcemark, LLC. 2 variants

SourceMark M0371 is a Class I device made by Sourcemark, LLC., listed in FDA GUDID since 26 Aug 2016 (UDI-DI 00897392000936), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00897392000936 UDI-DI Date26 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
SourceMark
Generic name
Laryngeal mask airway, reusable
Model / reference
M0371
Primary DI / UDI-DI
00897392000936
FDA product code
CAE
GMDN term
Laryngeal mask airway, reusable
Device class
Class I
Regulation number
868.5110
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laryngeal mask airway, reusable

Similar devices in this category

Other devices filed under Laryngeal mask airway, reusable.

Other devices from Sourcemark, LLC.

See all devices from Sourcemark, LLC. →

Properties

  • Supplied sterile
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)