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Panoview Plus Hd 892107253

by Richard Wolf GmbH

Ref 892107253Model 10000201216

Panoview Plus Hd 892107253 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-04055207035092) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04055207035092), 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-04055207035092 Basic UDI-DI 04055207035092UDI-DIDate4 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207035092 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207035092 registered 4 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207035092 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207035092
  2. Registered EUDAMED B-04055207035092

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  • Withdrawn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
Panoview Plus Hd
Generic name
Rigid endoscope telescope
Device name
Rigid Spine endosc. with working channel
Model / Ref / Catalog
892107253, 10000201216
Description
DISCOSCOPE 25° Ø 5.9MM SL 122MM rigid, with lateral ocular lens, working channel Ø 3.1mm, irrigation channel Ø 1.2mm, TL 236mm, rod lens system
Primary DI / UDI-DI
04055207035092
Basic UDI-DI
B-04055207035092
FDA product code
HRX
EMDN code
Z12020903 Spinoscopes
GMDN term
Rigid endoscope telescope
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
888.1100
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Angle — 25 degree
Length — 122 Millimeter
Outer Diameter — 5.9 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: Rigid endoscope telescope

Similar devices in this category

Other devices filed under NEUROENDOSCOPY INSTRUMENTS.

Other devices from Richard Wolf GmbH

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Properties

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