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Staminalift TS6000

by Staminalift International Limited

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB232TS60000 UDI-DI Date5 Apr 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Staminalift
Generic Name
Bed transporter
Model / Ref / Catalog
TS6000, STM684
Primary DI / UDI-DI
B232TS60000
FDA Product Code
FNL
GMDN Term
Bed transporter
Device Class
Class II
Regulation Number
880.5100
GUDID distribution status
In Commercial Distribution

Other devices from Staminalift International Limited

Properties

  • Contains Latex
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No