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Ex-Hex Definitive Abutment

by ZimVie US Corp LLC 3 variants

Part of a family of 98 devices: see the family page

Ref TUCA1

Ex-Hex Definitive Abutment (TUCA1) is a Class IIb device made by ZimVie US Corp LLC, registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI 844868DCJ5), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number844868DCJ5 Basic UDI-DI 00844868018865UDI-DIDate30 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Ex-Hex Definitive Abutment
Model / reference
TUCA1
Primary DI / UDI-DI
00844868018865
Basic UDI-DI
844868DCJ5
EMDN code
P01020101 Dental implants
Device class
Class IIb
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
US-MF-000048255
Authorised representative
ZimVie Spain S.L.U. ES-AR-000000983

Similar devices in this category

Other devices filed under DENTAL IMPLANTS.

Other devices from ZimVie US Corp LLC

See all devices from ZimVie US Corp LLC →

Properties

  • Sterilise before use
  • Implantable
  • Sutures
Other properties (12, all answered No)