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SCANLAN® Titanium Clamp 3003-59

by Scanlan International Inc

Ref 3003-59

SCANLAN® Titanium Clamp 3003-59 is a Class I device made by Scanlan International Inc, registered in EUDAMED on 18 May 2026 (Basic UDI-DI B-00846159033793) and listed in FDA GUDID since 1 Oct 2018 (UDI-DI 00846159033793), 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-00846159033793 Basic UDI-DI 00846159033793UDI-DIDate18 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00846159033793 UDI-DI Date1 Oct 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00846159033793 registered 18 May 2026 Active
  • FDA GUDID UDI-DI 00846159033793 listed 1 Oct 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00846159033793
  2. Registered EUDAMED B-00846159033793

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  • Withdrawn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® Titanium Clamp
Generic name
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Model / Ref / Catalog
3003-59
Primary DI / UDI-DI
00846159033793
Basic UDI-DI
B-00846159033793
FDA product code
GDJ
EMDN code
L031306 Hemostatic forceps, reusable
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device class
Class I
Regulation number
878.4800
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

Related devices

Category: Surgical soft-tissue manipulation forceps, scissors-like, 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)