D-Camsource® CSDS6000N

D-Camsource® CSDS6000N is a Class I device made by Joimax GmbH, listed in FDA GUDID since 30 Dec 2022 (UDI-DI 04250337119920), registry data as of 12 Nov 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

Source GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04250337119920 UDI-DI	Date30 Dec 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04250337119920

Coverage

1 jurisdiction

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Withdrawn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: CSDS6000N

Primary DI / UDI-DI: 04250337119920
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

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Properties

Prescription use
Premarket exempt
Serial number
Manufacturing date

Other properties (11, all answered No)