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SemiCut

EUDAMED

Class IIa (EU MDR)

Ref PD0PP1812

by M.D.L. S.r.l.

Identity

Trade Name
SemiCut EUDAMED
Device Name
SemiCut EUDAMED
Model / Reference
PD0PP1812 EUDAMED

Identifiers

Primary DI / UDI-DI
08057276004333 EUDAMED
Basic UDI-DI
B-08057276004333 EUDAMED
EMDN Code
A0102010101 SHEARING BIOPSY NEEDLES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

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

SemiCut by M.d.l. S.r.l. — Class IIa — 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
M.D.L. S.r.l.
EUDAMED SRN
IT-MF-000011599

Sources (1)

  • EUDAMED 267dc19f-036c-46c7-af68-674f97061386 61 fields · synced May 23, 2026