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Endocam 85525902

by Richard Wolf GmbH

Ref 85525902Model 10000201142

Endocam 85525902 is an endoscope video camera (EU MDR Class I; FDA Class II; FDA product code FET, Endoscopic video imaging system/component, gastroenterology-urology) made by Richard Wolf GmbH, registered in EUDAMED on 4 Dec 2025 (Basic UDI-DI 405520724072019-0017775NA) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04055207027370), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number405520724072019-0017775NA Basic UDI-DI 04055207027370UDI-DIDate4 Dec 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207027370 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 405520724072019-0017775NA registered 4 Dec 2025 Active
  • FDA GUDID UDI-DI 04055207027370 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207027370
  2. Registered EUDAMED 405520724072019-0017775NA

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  • Withdrawn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
Endocam
Generic name
Endoscope video camera
Device name
Camera heads
Model / Ref / Catalog
85525902, 10000201142
Description
LOGIC HD CAMERA HEAD CABLE 3M C-Mount, 1 chip, 2 camera-head buttons, Sensor size: 1/3"
Primary DI / UDI-DI
04055207027370
Basic UDI-DI
405520724072019-0017775NA
Direct marketing DI
04055207027370
FDA product code
FET
EMDN code
Z12020405 Surgical cameras
GMDN term
Endoscope video camera
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Endoscope video camera

Similar devices in this category

Other devices filed under SURGICAL CAMERAS.

Other devices from Richard Wolf GmbH

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Properties

  • Sterilise before use
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)