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Newclip Instruments ANC019

by Newclip Technics

Part of a family of 60 devices: see the family page

Ref ANC019

Newclip Instruments ANC019 is a Class I device made by Newclip Technics, registered in EUDAMED on 2 Jul 2026 (Basic UDI-DI 3700569600418W) and listed in FDA GUDID since 7 Nov 2024 (UDI-DI 03700569619190), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number3700569600418W Basic UDI-DI 03700569619190UDI-DIDate2 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03700569619190 UDI-DI Date7 Nov 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 3700569600418W registered 2 Jul 2026 Active
  • FDA GUDID UDI-DI 03700569619190 listed 7 Nov 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03700569619190
  2. Registered EUDAMED 3700569600418W

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Newclip Instruments
Generic name
Bone lever/elevator, reusable
Device name
Instruments for trauma and orthopaedic surgery
Model / Ref / Catalog
ANC019
Primary DI / UDI-DI
03700569619190
Basic UDI-DI
3700569600418W
FDA product code
HTZ
EMDN code
L0923 Orthopaedics surgical measurers, reusable
GMDN term
Bone lever/elevator, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone lever/elevator, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDICS SURGICAL MEASURERS, REUSABLE.

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Properties

  • Sterilise before use
  • Reusable
  • Measuring function
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)