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Newclip Instruments ANC1104

by Newclip Technics

Ref ANC1104

Newclip Instruments ANC1104 is a Class I device made by Newclip Technics, registered in EUDAMED on 16 Jul 2026 (Basic UDI-DI 37005696003695) and listed in FDA GUDID since 7 Nov 2024 (UDI-DI 03700569631062), 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 Number37005696003695 Basic UDI-DI 03700569631062UDI-DIDate16 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03700569631062 UDI-DI Date7 Nov 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 37005696003695 registered 16 Jul 2026 Active
  • FDA GUDID UDI-DI 03700569631062 listed 7 Nov 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03700569631062
  2. Registered EUDAMED 37005696003695

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  • Withdrawn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 holding forceps
Device name
Instruments used in trauma and orthopaedic surgery
Model / Ref / Catalog
ANC1104
Primary DI / UDI-DI
03700569631062
Basic UDI-DI
37005696003695
FDA product code
HTZ
EMDN code
L091399 Orthopaedic surgery forceps, reusable - other
GMDN term
Bone holding forceps
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 holding forceps

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY FORCEPS, REUSABLE - OTHER.

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Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)