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St-1000_V2

by Shinyoung for M Co., Ltd.

St-1000_V2 is a Class I device made by Shinyoung for M Co., Ltd., listed in FDA GUDID since 20 Nov 2023 (UDI-DI 08809832900012), 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 Number08809832900012 UDI-DI Date20 Nov 2023ListedStatusListed 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  • Withdrawn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
St-1000
Generic name
Examination/operating table component trolley
Model / reference
ST-1000_V2
Primary DI / UDI-DI
08809832900012
FDA product code
LGX
GMDN term
Examination/operating table component trolley
Device class
Class I
Regulation number
878.4960
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LGX (Table, Examination, Medical, Powered).

Other devices from Shinyoung for M Co., Ltd.

See all devices from Shinyoung for M Co., Ltd. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)