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SCANLAN® Super Cut™ 7007-252-1SC

by Scanlan International Inc

Ref 7007-252-1SC

SCANLAN® Super Cut™ 7007-252-1SC is a Class I device made by Scanlan International Inc, registered in EUDAMED on 18 May 2026 (Basic UDI-DI B-00846159030907) and listed in FDA GUDID since 23 Mar 2016 (UDI-DI 00846159030907), 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-00846159030907 Basic UDI-DI 00846159030907UDI-DIDate18 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00846159030907 UDI-DI Date23 Mar 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00846159030907 registered 18 May 2026 Active
  • FDA GUDID UDI-DI 00846159030907 listed 23 Mar 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00846159030907
  2. Registered EUDAMED B-00846159030907

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  • Withdrawn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® Super Cut™
Generic name
General-purpose surgical scissors, reusable
Device name
SCANLAN® Diethrich‑Potts Scissors
Model / Ref / Catalog
7007-252-1SC
Primary DI / UDI-DI
00846159030907
Basic UDI-DI
B-00846159030907
FDA product code
LRW
EMDN code
L01040402 Vascular scissors, reusable
GMDN term
General-purpose surgical scissors, 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: General-purpose surgical scissors, reusable

Similar devices in this category

Other devices filed under SURGICAL SCISSORS, 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)