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Newclip Instruments ANC1105

by Newclip Technics

Ref ANC1105

Newclip Instruments ANC1105 is a Class I device made by Newclip Technics, registered in EUDAMED on 16 Jul 2026 (Basic UDI-DI 3700569600128P) and listed in FDA GUDID since 7 Nov 2024 (UDI-DI 03700569631079), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number3700569600128P Basic UDI-DI 03700569631079UDI-DIDate16 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03700569631079 UDI-DI Date7 Nov 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 3700569600128P registered 16 Jul 2026 Active
  • FDA GUDID UDI-DI 03700569631079 listed 7 Nov 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03700569631079
  2. Registered EUDAMED 3700569600128P

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  • Withdrawn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
Surgical implant/trial-implant/sizer holder, reusable
Device name
Instruments used in trauma and orthopaedic surgery
Model / Ref / Catalog
ANC1105
Primary DI / UDI-DI
03700569631079
Basic UDI-DI
3700569600128P
FDA product code
HTZ
EMDN code
L091301 Bone grasps, reusable
GMDN term
Surgical implant/trial-implant/sizer holder, 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: Surgical implant/trial-implant/sizer holder, reusable

Similar devices in this category

Other devices filed under BONE GRASPS, REUSABLE.

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Properties

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