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Hopkins 7230FVA

by Karl Storz SE & CO. KG

Part of a family of 33 devices: see the family page

Ref 7230FVA

Hopkins 7230FVA is a device classified as Class IIa in the EU and Class II in the US made by Karl Storz SE & CO. KG, registered in EUDAMED on 19 May 2026 (Basic UDI-DI 4048551001416TN) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551194041), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4048551001416TN Basic UDI-DI 04048551194041UDI-DIDate19 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04048551194041 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4048551001416TN registered 19 May 2026 Active
  • FDA GUDID UDI-DI 04048551194041 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04048551194041
  2. Registered EUDAMED 4048551001416TN

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  • Withdrawn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

Trade name
Hopkins
Generic name
Rigid optical rhinoscope
Device name
Rigid telescopes
Model / reference
7230FVA
Primary DI / UDI-DI
04048551194041
Basic UDI-DI
4048551001416TN
FDA product code
EOB
EMDN code
Z12021008 Rhinoscopes
GMDN term
Rigid optical rhinoscope
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
874.4760
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

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 optical rhinoscope

Similar devices in this category

Other devices filed under ENT ENDOSCOPY INSTRUMENTS.

Other devices from Karl Storz SE & CO. KG

See all devices from Karl Storz SE & CO. KG →

Properties

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