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Aoj-50C

by Shenzhen AOJ Medical Technology Co., Ltd

Aoj-50C is a Class II device made by Shenzhen AOJ Medical Technology Co., Ltd, listed in FDA GUDID since 26 Jan 2021 (UDI-DI 06972040110534), 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 Number06972040110534 UDI-DI Date26 Jan 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  • Withdrawn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

Generic name
Foetal cardiac monitor
Model / reference
AOJ-50C
Primary DI / UDI-DI
06972040110534
FDA product code
KNG
GMDN term
Foetal cardiac monitor
Device class
Class II
Regulation number
884.2660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Foetal cardiac monitor

Other devices from Shenzhen AOJ Medical Technology Co., Ltd

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

Properties

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