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Cogent E300

by Fu Shun Hsing Technology Co., Ltd.

Cogent E300 is a Class II device made by Fu Shun Hsing Technology Co., Ltd., listed in FDA GUDID since 20 Sep 2016 (UDI-DI 04713157963000), 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 Number04713157963000 UDI-DI Date20 Sep 2016ListedStatusListed 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  • Withdrawn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
Cogent
Generic name
Bathing stretcher
Model / reference
E300
Primary DI / UDI-DI
04713157963000
FDA product code
FPO
GMDN term
Bathing stretcher
Device class
Class II
Regulation number
880.6910
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FPO (Stretcher, Wheeled).

Other devices from Fu Shun Hsing Technology Co., Ltd.

See all devices from Fu Shun Hsing Technology Co., Ltd. →

Properties

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