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Cogent E200

by Fu Shun Hsing Technology Co., Ltd.

Cogent E200 is a hospital stretcher (FDA Class II; FDA product code FPO, Stretcher, Wheeled) made by Fu Shun Hsing Technology Co., Ltd., listed in FDA GUDID since 20 Sep 2016 (UDI-DI 04713157962263), 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 Number04713157962263 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  • Withdrawn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
Hospital stretcher, manual
Model / reference
E200
Primary DI / UDI-DI
04713157962263
FDA product code
FPO
GMDN term
Hospital stretcher, manual
Device class
Class II
Regulation number
880.6910
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hospital stretcher, manual

Similar devices in this category

Other devices filed under Hospital stretcher, manual.

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

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Properties

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