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Wisonic G60

by Shenzhen Wisonic Medical Technology Co., Ltd.

Wisonic G60 is a Class II device made by Shenzhen Wisonic Medical Technology Co., Ltd., listed in FDA GUDID since 29 Jan 2019 (UDI-DI 06971355420253), 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 Number06971355420253 UDI-DI Date29 Jan 2019ListedStatusListed 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  • Withdrawn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
Wisonic
Generic name
Electromechanical device/system transport trolley
Model / reference
G60
Primary DI / UDI-DI
06971355420253
FDA product code
ITX, IYN, IYO
GMDN term
Electromechanical device/system transport trolley
Device class
Class II
Regulation number
892.1570, 892.1550, 892.1560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electromechanical device/system transport trolley

Similar devices in this category

Other devices filed under Electromechanical device/system transport trolley.

Other devices from Shenzhen Wisonic Medical Technology Co., Ltd.

See all devices from Shenzhen Wisonic Medical Technology Co., Ltd. →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)