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95-3930

by SCHÖLLY FIBEROPTIC GmbH

Ref 95-3930Model Camera Control Units

95-3930 is a device classified as Class I in the EU and Class II in the US made by SCHÖLLY FIBEROPTIC GmbH, registered in EUDAMED on 12 Mar 2026 (Basic UDI-DI 42504801CCUSGN) and listed in FDA GUDID since 15 Feb 2019 (UDI-DI 04250480107027), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42504801CCUSGN Basic UDI-DI Date12 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250480107027 UDI-DI Date15 Feb 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42504801CCUSGN registered 12 Mar 2026 Active
  • FDA GUDID UDI-DI 04250480107027 listed 15 Feb 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250480107027
  2. Registered EUDAMED 42504801CCUSGN

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  • Withdrawn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

Generic name
Endoscope video camera
Model / reference
95-3930, Camera Control Units
Primary DI / UDI-DI
04250480107027, 04250480112861, 04250480102251
Basic UDI-DI
42504801CCUSGN
Direct marketing DI
04250480102251
04250480112861
04250480107027
FDA product code
GCJ, FET, OWN
EMDN code
Z12020406 Video processors
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
MRI safety
MR Unsafe

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 VIDEO PROCESSORS.

Other devices from SCHÖLLY FIBEROPTIC GmbH

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See all devices from SCHÖLLY FIBEROPTIC GmbH →

Properties

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