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SourceMark M0910

by Sourcemark, LLC. 3 variants

SourceMark M0910 is a Class I device made by Sourcemark, LLC., listed in FDA GUDID since 7 Jul 2020 (UDI-DI 00813799000065), 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 Number00813799000065 UDI-DI Date7 Jul 2020ListedStatusListed 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  • Withdrawn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
Artificial airway stylet, single-use
Model / reference
M0910
Primary DI / UDI-DI
00813799000065
FDA product code
BSR
GMDN term
Artificial airway stylet, single-use
Device class
Class I
Regulation number
868.5790
GUDID distribution status
In Commercial Distribution

Related devices

Category: Artificial airway stylet, single-use

Other devices from Sourcemark, LLC.

See all devices from Sourcemark, LLC. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)