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SCANLAN® Titanium Forceps 3003-770

by Scanlan International Inc

Ref 3003-770

SCANLAN Titanium Forceps 3003-770 is a surgical soft-tissue manipulation forceps (EU MDD Class I; FDA Class I; FDA product code GZX, Instrument, Microsurgical) made by Scanlan International Inc, registered in EUDAMED on 18 May 2026 (Basic UDI-DI B-00846159003659) and listed in FDA GUDID since 5 Nov 2019 (UDI-DI 00846159003659), 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-00846159003659 Basic UDI-DI 00846159003659UDI-DIDate18 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00846159003659 UDI-DI Date5 Nov 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00846159003659 registered 18 May 2026 Active
  • FDA GUDID UDI-DI 00846159003659 listed 5 Nov 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00846159003659
  2. Registered EUDAMED B-00846159003659

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  • Withdrawn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 Forceps
Generic name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device name
SCANLAN® Puskas™ Micro Forceps
Model / Ref / Catalog
3003-770
Primary DI / UDI-DI
00846159003659
Basic UDI-DI
B-00846159003659
FDA product code
GZX
EMDN code
L031306 Hemostatic forceps, reusable
GMDN term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device class
Class I
Regulation number
882.4525
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, tweezers-like, reusable

Similar devices in this category

Other devices filed under HEMOSTATIC FORCEPS, REUSABLE.

Other devices from Scanlan International Inc

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Properties

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