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Camsource® CSFHD01CO

by Joimax GmbH

Ref CSFHD01CO

Camsource® CSFHD01CO is a Class I device made by Joimax GmbH, registered in EUDAMED on 21 May 2026 (Basic UDI-DI 42503371C+FUCOX8) and listed in FDA GUDID since 30 Dec 2022 (UDI-DI 04250337115236), active as of 12 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42503371C+FUCOX8 Basic UDI-DI 04250337115236UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250337115236 UDI-DI Date30 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42503371C+FUCOX8 registered 21 May 2026 Active
  • FDA GUDID UDI-DI 04250337115236 listed 30 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250337115236
  2. Registered EUDAMED 42503371C+FUCOX8

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Camera Head Ocular for Camsource® LED EUDAMED
Camsource® GUDID
Generic name
Endoscopic video image processing/light source system
Model / Ref / Catalog
CSFHD01CO
Primary DI / UDI-DI
04250337115236
Basic UDI-DI
42503371C+FUCOX8
Direct marketing DI
04250337115236
FDA product code
FWF
EMDN code
Z12020402, Z12020405
GMDN term
Endoscopic video image processing/light source system
Device class
Class I
Regulation number
878.4160
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Sterilise before useEUDAMED
No
GUDID
Yes

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 04250337115236: EUDAMED states No, FDA GUDID states Yes.

Related devices

Category: Endoscopic video image processing/light source system

Similar devices in this category

Other devices filed under LIGHT SOURCES FOR ENDOSCOPY AND MINIMALLY INVASIVE SURGERY.

Other devices from Joimax GmbH

See all devices from Joimax GmbH →

Properties

  • Sterilise before use NoEUDAMEDYesGUDID
  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (20, all answered No)