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Mamba 7315001

by Richard Wolf GmbH

Ref 7315001Model 10000201435

Mamba 7315001 is a flexible video cystoscope (EU MDD Class IIa; FDA Class II; FDA product code FAJ, Cystoscope and accessories, flexible/rigid) made by Richard Wolf GmbH, registered in EUDAMED on 4 Sep 2026 (Basic UDI-DI B-04055207063460) and listed in FDA GUDID since 10 Apr 2018 (UDI-DI 04055207063460), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04055207063460 Basic UDI-DI 04055207063460UDI-DIDate4 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207063460 UDI-DI Date10 Apr 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207063460 registered 4 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207063460 listed 10 Apr 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207063460
  2. Registered EUDAMED B-04055207063460

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  • Withdrawn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
Mamba
Generic name
Flexible video cystoscope, reusable
Device name
Sensor cystoscopes with working channel
Model / Ref / Catalog
7315001, 10000201435
Primary DI / UDI-DI
04055207063460
Basic UDI-DI
B-04055207063460
FDA product code
FAJ
EMDN code
Z12020701 Cystoscopes
GMDN term
Flexible video cystoscope, reusable
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 — 5.4 Millimeter
Length — 400 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
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 video cystoscope, reusable

Similar devices in this category

Other devices filed under CYSTOSCOPES.

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)