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Coxo C-Fill

by Foshan COXO Medical Instrument Co., Ltd.

Ref C-FillModel C-FiII

Coxo C-Fill is an endodontic obturation system (EU MDR Class IIa; FDA Class I; FDA product code EIY, Instrument, Filling, Plastic, Dental) made by Foshan COXO Medical Instrument Co., Ltd., registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI 697426789172A) and listed in FDA GUDID since 18 Dec 2024 (UDI-DI 16974267898285), 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 Number697426789172A Basic UDI-DI 16974267898285UDI-DIDate16 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number16974267898285 UDI-DI Date18 Dec 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 697426789172A registered 16 Oct 2026 Active
  • FDA GUDID UDI-DI 16974267898285 listed 18 Dec 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 16974267898285
  2. Registered EUDAMED 697426789172A

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  • Withdrawn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
Coxo
Generic name
Endodontic obturation system
Model / reference
C-FILL, C-FiII
Primary DI / UDI-DI
16974267898285 EUDAMED
06974267890572 GUDID
Basic UDI-DI
697426789172A
FDA product code
EIY
EMDN code
Z12119099 Various dental stomatology instruments - other
GMDN term
Endodontic obturation system
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
872.4565
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
16974267898285
GUDID
06974267890572
Device classEUDAMED
Class IIa
GUDID
Class I
Supplied sterileEUDAMED
Yes
GUDID
No

The registries describe this device under different primary UDI-DIs (EUDAMED lists 16974267898285; FDA GUDID lists 06974267890572), so their flags are not compared. Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Endodontic obturation system

Similar devices in this category

Other devices filed under VARIOUS DENTAL STOMATOLOGY INSTRUMENTS - OTHER.

Other devices from Foshan COXO Medical Instrument Co., Ltd.

See all devices from Foshan COXO Medical Instrument Co., Ltd. →

Properties

  • Supplied sterile YesEUDAMEDNoGUDID
  • Sterilise before use
  • Reusable
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (18, all answered No)