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Ortholoc® 3Di

by Wright Medical Technology, Inc. United States EUDAMED

Ref 5852006LModel 08858251006564TZ EMDN P09120503

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08858251006564TZ Basic UDI-DIDate7 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Ortholoc 3DI Plantar Lapidus Implants - Plantar Lapidus Plate - Titanium Alloy - Class Iib- Nonsterile
Model / Reference
08858251006564TZ, 5852006L
Primary DI / UDI-DI
00840420172174
Basic UDI-DI
08858251006564TZ
EMDN Code
P09120503 Osteosynthesis screw-plate systems
Device Class
Class IIb
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000025260
Authorised representative
Stryker European Operations Limited IE-AR-000000092

Other devices from Wright Medical Technology, Inc.

See all devices from Wright Medical Technology, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Implantable
  • Sutures
Other properties (12)
  • Sterile: 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

Sources (1)

  • EUDAMED 00840420172174|08858251006564TZ 61 fields · synced 24 Oct 2026