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Instrumentation class I

by Newclip Technics SAS 47 variants

Part of a family of 131 devices: see the family page

Ref ANC791/B

Instrumentation class I (ANC791/B) is a Class I device made by Newclip Technics SAS, registered in EUDAMED on 12 May 2026 (Basic UDI-DI 37005696004494) and listed in FDA GUDID since 12 May 2026 (UDI-DI 03700569657154), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number37005696004494 Basic UDI-DI 03700569657154UDI-DIDate12 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03700569657154 UDI-DI Date12 May 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 37005696004494 registered 12 May 2026 Active
  • FDA GUDID UDI-DI 03700569657154 listed 12 May 2026 Listed

Timeline

2 dated events

  1. Registered EUDAMED 37005696004494
  2. Listed FDA GUDID 03700569657154

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  • Withdrawn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
Instrument tray, reusable
Device name
Instrumentation class I
Model / Ref / Catalog
ANC791/B
Primary DI / UDI-DI
03700569657154
Basic UDI-DI
37005696004494
FDA product code
FSM
EMDN code
V0402 Clinical use trays and bowls
GMDN term
Instrument tray, 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

Manufacturer details

EUDAMED SRN
FR-MF-000011809

Similar devices in this category

Other devices filed under CLINICAL USE TRAYS AND BOWLS.

Other devices from Newclip Technics SAS

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Properties

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