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Panoview Plus 82514431

by Richard Wolf GmbH

Ref 82514.431Model 10000201539

Panoview Plus 82514431 (82514.431) 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 26 Oct 2026 (Basic UDI-DI B-04055207026441) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04055207026441), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04055207026441 Basic UDI-DI 04055207026441UDI-DIDate26 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207026441 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207026441 registered 26 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207026441 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207026441
  2. Registered EUDAMED B-04055207026441

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  • Withdrawn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
Generic name
Rigid endoscope telescope
Device name
Rigid endoscopes without working channel
Model / Ref / Catalog
10000201539, 82514.431, 82514431
Description
TELESCOPE 0° Ø 4MM WL 519MM rigid, TL 388mm, rod lens system
Primary DI / UDI-DI
04055207026441
Basic UDI-DI
B-04055207026441
FDA product code
HET
EMDN code
Z12020801 Bronchoscopes
GMDN term
Rigid endoscope telescope
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
884.1720
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
Length — 519 Millimeter
Outer Diameter — 4 Millimeter
Angle — 0 degree

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201539
82514.431
GUDID
82514431
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.

Similar devices in this category

Other devices filed under BRONCHOSCOPES.

Other devices from Richard Wolf GmbH

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Properties

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