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SourceMark SLMIL30

by Sourcemark, LLC.

SourceMark SLMIL30 is a Class I device made by Sourcemark, LLC., listed in FDA GUDID since 4 Dec 2020 (UDI-DI 00813799003639), 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 Number00813799003639 UDI-DI Date4 Dec 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  • Withdrawn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
Flexible fibreoptic laryngoscope
Model / reference
SLMIL30
Primary DI / UDI-DI
00813799003639
FDA product code
CCW
GMDN term
Flexible fibreoptic laryngoscope
Device class
Class I
Regulation number
868.5540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Flexible fibreoptic laryngoscope

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)