Skip to content

Viper 7325071

by Richard Wolf GmbH

Ref 7325.071Model 10000201436

Viper 7325071 (7325.071) is a device classified as Class IIa in the EU and Class II in the US made by Richard Wolf GmbH, registered in EUDAMED on 4 Sep 2026 (Basic UDI-DI B-04055207013694) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04055207013694), active as of 25 Oct 2026.

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

CE MDD

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/MDD EUDAMED NumberB-04055207013694 Basic UDI-DI 04055207013694UDI-DIDate4 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207013694 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207013694 registered 4 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207013694 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207013694
  2. Registered EUDAMED B-04055207013694

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Viper
Generic name
Flexible fibreoptic ureterorenoscope
Device name
Flex. ureterorenosc. with work. channel
Model / Ref / Catalog
10000201436, 7325.071, 7325071
Primary DI / UDI-DI
04055207013694
Basic UDI-DI
B-04055207013694
FDA product code
FAJ
EMDN code
Z12020713 Ureterorenoscopes
GMDN term
Flexible fibreoptic ureterorenoscope
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
876.1500
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Hydrogen Peroxide
Size
Outer Diameter — 3.2 Millimeter
Length — 680 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201436
7325.071
GUDID
7325071
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa 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: Flexible fibreoptic ureterorenoscope

Similar devices in this category

Other devices filed under URETERORENOSCOPES.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

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