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SourceMark M1030

by Sourcemark, LLC. 2 variants

SourceMark M1030 is a Class I device made by Sourcemark, LLC., listed in FDA GUDID since 9 Jul 2020 (UDI-DI 00813799006104), 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 Number00813799006104 UDI-DI Date9 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  • Withdrawn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
Nasopharyngeal airway, single-use
Model / reference
M1030
Primary DI / UDI-DI
00813799006104
FDA product code
BTQ
GMDN term
Nasopharyngeal airway, single-use
Device class
Class I
Regulation number
868.5100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nasopharyngeal airway, single-use

Similar devices in this category

Other devices filed under Nasopharyngeal airway, 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)