← Back to catalogue

Ortimplant

EUDAMED

Class IIb (EU MDR)

Ref O6014050

by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi

Identity

Trade Name
Ortimplant EUDAMED
Device Name
4,0 MM BAŞSIZ KANÜLLÜ KOMPRESYON VİDASI TİTANYUM (4,0 MM HEADLESS CANNULATED COMPRESSION SCREW TITANIUM) 50 MM EUDAMED
Model / Reference
O6014050 EUDAMED

Identifiers

Primary DI / UDI-DI
08680941153021 EUDAMED
Basic UDI-DI
B-08680941153021 EUDAMED
EMDN Code
P09120201 INTRAMEDULLARY NAILS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Arthrodesis intramedullary nail, non-distracting

Ortimplant by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Arthrodesis intramedullary nail, non-distracting.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
TR-MF-000017438

Sources (1)

  • EUDAMED 0bccb980-c28e-41b2-8c24-c13ef902de3c 61 fields · synced Jun 20, 2026