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fX

EUDAMED

Class III (EU MDR)

Ref SCRW-FXPT30IS630

by Bonegraft Biomaterials Co.

Identity

Trade Name
fX EUDAMED
Device Name
fX® PLDLLA+TCP 30 Interference Screws Ø 6mm x 30mm EUDAMED
Model / Reference
SCRW-FXPT30IS630 EUDAMED

Identifiers

Primary DI / UDI-DI
08681781339569 EUDAMED
Basic UDI-DI
B-08681781339569 EUDAMED
EMDN Code
P09120605 INTERFERENCE SCREWS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Tendon/ligament bone anchor, non-bioabsorbable

fX by Bonegraft Biomaterials Co. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000015715

Sources (1)

  • EUDAMED 89bdf8ef-5e8d-4817-b30b-763db3c37694 61 fields · synced Jun 19, 2026