Skip to content

Aequalis® Fracture

by Tornier SAS

Ref YRAD30Model 08858251006896UV

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08858251006896UV Basic UDI-DI 03700434014280UDI-DIDate6 Oct 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Tornier SAS Class I Devices - Trays and Tray Accessories - Class I - Non Sterile
Model / Reference
08858251006896UV, YRAD30
Primary DI / UDI-DI
03700434014280
Basic UDI-DI
08858251006896UV
Direct Marketing DI
03700434014280
EMDN Code
V0402 Clinical use trays and bowls
Device Class
Class I
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
FR-MF-000011808

Other devices from Tornier SAS

See all devices from Tornier SAS →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No