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E-Line 8677254

by Richard Wolf GmbH

Ref 8677.254Model 10000201472

E-Line 8677254 (8677.254) is a pin-indexed adaptor (EU MDR Class I; FDA Class II; FDA product code FDC, Resectoscope, Working Element) made by Richard Wolf GmbH, registered in EUDAMED on 8 Nov 2025 (Basic UDI-DI 405520727052019-0028583QC) and listed in FDA GUDID since 26 Sep 2016 (UDI-DI 04055207019771), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number405520727052019-0028583QC Basic UDI-DI 04055207019771UDI-DIDate8 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207019771 UDI-DI Date26 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 405520727052019-0028583QC registered 8 Nov 2025 Active
  • FDA GUDID UDI-DI 04055207019771 listed 26 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207019771
  2. Registered EUDAMED 405520727052019-0028583QC

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  • Withdrawn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
E-Line
Generic name
Pin-indexed adaptor, reusable
Device name
Adapters
Model / Ref / Catalog
10000201472, 8677.254, 8677254
Primary DI / UDI-DI
04055207019771
Basic UDI-DI
405520727052019-0028583QC
Direct marketing DI
04055207019771
FDA product code
FDC
EMDN code
L060413 Endoscopic urology adapters and connectors, reusable
GMDN term
Pin-indexed adaptor, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201472
8677.254
GUDID
8677254
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Pin-indexed adaptor, reusable

Similar devices in this category

Other devices filed under ENDOSCOPIC UROLOGY INSTRUMENTS, REUSABLE.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

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