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Scanlan® 3785-41

by Scanlan International Inc

Ref 3785-41

Scanlan® 3785-41 is a device classified as Class I in the EU and Class II in the US made by Scanlan International Inc, registered in EUDAMED on 18 May 2026 (Basic UDI-DI B-00846159029406) and listed in FDA GUDID since 5 Jan 2016 (UDI-DI 00846159029406), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00846159029406 Basic UDI-DI 00846159029406UDI-DIDate18 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00846159029406 UDI-DI Date5 Jan 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00846159029406 registered 18 May 2026 Active
  • FDA GUDID UDI-DI 00846159029406 listed 5 Jan 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00846159029406
  2. Registered EUDAMED B-00846159029406

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  • Withdrawn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
Scanlan®
Generic name
Surgical bulldog clamp, reusable
Device name
SCANLAN® Yasargil Temporary Occlusion Clip
Model / Ref / Catalog
3785-41
Primary DI / UDI-DI
00846159029406
Basic UDI-DI
B-00846159029406
FDA product code
DXC
EMDN code
L031306 Hemostatic forceps, reusable
GMDN term
Surgical bulldog clamp, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
870.4450
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
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 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: Surgical bulldog clamp, reusable

Similar devices in this category

Other devices filed under HEMOSTATIC FORCEPS, REUSABLE.

Other devices from Scanlan International Inc

See all devices from Scanlan International Inc →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)