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MY SCREW Ø2.5 Lg 20

EUDAMED

Class IIb (EU MDR)

Ref 38.88.20Model MY SCREW

by Ortho Cape

Identity

Trade Name
MY SCREW Ø2.5 Lg 20 EUDAMED
Device Name
MY SCREW Ø2.5 Lg 20mm EUDAMED
Model / Reference
MY SCREW EUDAMED
38.88.20 EUDAMED

Identifiers

Primary DI / UDI-DI
03760347451398 EUDAMED
Basic UDI-DI
B-03760347451398 EUDAMED
EMDN Code
P09120603 CANNULATED SCREWS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

Yes

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

MY SCREW Ø2.5 Lg 20 by Ortho Cape — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Ortho Cape
EUDAMED SRN
FR-MF-000028862

Sources (1)

  • EUDAMED d45de20f-8e03-4ff7-bc38-3b1259792f9e 61 fields · synced Jun 19, 2026