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D-Camsource® CSDHDU80P

by Joimax, Inc.

D-Camsource® CSDHDU80P is a Class I device made by Joimax, Inc., listed in FDA GUDID since 30 Dec 2022 (UDI-DI 04250337106180), 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 Number04250337106180 UDI-DI Date30 Dec 2022ListedStatusListed 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  • Withdrawn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
D-Camsource®
Generic name
Endoscopic video image processing/light source system
Model / Ref / Catalog
CSDHDU80P
Primary DI / UDI-DI
04250337106180
FDA product code
FWF
GMDN term
Endoscopic video image processing/light source system
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic video image processing/light source system

Other devices from Joimax, Inc.

See all devices from Joimax, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)