Ortimplant

by Ortimplant Ortopedi ve Tıbbi Aletleri Sanayi Ticaret Limited Şirketi 1,000+ variants

Ref O110 03 226 0700

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-08680941146351 Basic UDI-DI 08680941146351UDI-DI	Date19 Mar 2024Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: 6,5 Mm Spongioz Vİda 32 Mm Yi̇vli̇ Ti̇tanyum (6,5 Mm Cancellous Screw 32 Mm Threaded Titanium) 70 Mm
Model / Reference: O110 03 226 0700

Primary DI / UDI-DI: 08680941146351
Basic UDI-DI: B-08680941146351
EMDN Code: P09120201 Intramedullary nails

Device Class: Class IIb
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000017438

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Properties

Implantable

Other properties (10)

Sterile: No
Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No