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MedSource Patient Mover MS-95206

by Medsource International LLC

MedSource Patient Mover MS-95206 (Not Applicable) is a Class I device made by Medsource International LLC, listed in FDA GUDID since 26 Jul 2021 (UDI-DI 00840155405998), 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 Number00840155405998 UDI-DI Date26 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  • Withdrawn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 Patient Mover
Generic name
Portable stretcher
Model / Ref / Catalog
MS-95206, Not Applicable
Primary DI / UDI-DI
00840155405998
FDA product code
FMR
GMDN term
Portable stretcher
Device class
Class I
Regulation number
880.6785
GUDID distribution status
In Commercial Distribution

Related devices

Category: Portable stretcher

Other devices from Medsource International LLC

See all devices from Medsource International LLC →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)