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Olympus A3555

by Olympus Winter & Ibe GmbH

Ref A3555

Olympus A3555 is a device classified as Class IIa in the EU and Class II in the US made by Olympus Winter & Ibe GmbH, registered in EUDAMED on 24 Sep 2026 (Basic UDI-DI B-04042761005272), cleared under FDA 510(k) K904940 on 13 Jan 1992 and listed in FDA GUDID since 22 Sep 2016 (UDI-DI 04042761005272), active as of 25 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDD 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K904940

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04042761005272 Basic UDI-DI 04042761005272UDI-DIDate24 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04042761005272 UDI-DI Date22 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK904940 Date13 Jan 1992DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-04042761005272 registered 24 Sep 2026 Active
  • FDA 510(k) K904940 decided 13 Jan 1992 Active
  • FDA GUDID UDI-DI 04042761005272 listed 22 Sep 2016 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K904940
  2. Listed FDA GUDID 04042761005272
  3. Registered EUDAMED B-04042761005272

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Knife, lancet type, for A3550 EUDAMED
Olympus GUDID
Generic name
Manual scalpel blade, reusable
Model / Ref / Catalog
A3555
Primary DI / UDI-DI
04042761005272
Basic UDI-DI
B-04042761005272
510(k) Number
FDA product code
FJL
EMDN code
L06040501 Endoscopic surgery urethrotomes and ureterotomes, reusable
GMDN term
Manual scalpel blade, 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
Moist Heat or Steam Sterilization

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: Manual scalpel blade, reusable

Cleared under the same submission (K904940)

and 5 more cleared under K904940

Similar devices in this category

Other devices filed under ENDOSCOPIC UROLOGY INSTRUMENTS, REUSABLE.

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See all devices from Olympus Winter & Ibe GmbH →

Properties

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