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MedSource Intubation Kit MS-B3351-USA

by Medsource International LLC

MedSource Intubation Kit MS-B3351-USA (Not Applicable) is a device made by Medsource International LLC, listed in FDA GUDID since 28 Jul 2021 (UDI-DI 00840155407497), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840155407497 UDI-DI Date28 Jul 2021ListedStatusListed 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  • Withdrawn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
MedSource Intubation Kit
Generic name
Retrograde endotracheal intubation kit
Model / Ref / Catalog
MS-B3351-USA, Not Applicable
Primary DI / UDI-DI
00840155407497
GMDN term
Retrograde endotracheal intubation kit
GUDID distribution status
In Commercial Distribution

Related devices

Category: Retrograde endotracheal intubation kit

Other devices from Medsource International LLC

See all devices from Medsource International LLC →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)