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CytoCut

EUDAMED

Class IIa (EU MDR)

Ref PB1910

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

Identity

Trade Name
CytoCut EUDAMED
Device Name
CytoCut EUDAMED
Model / Reference
PB1910 EUDAMED

Identifiers

Primary DI / UDI-DI
08055271571799 EUDAMED
Basic UDI-DI
B-08055271571799 EUDAMED
EMDN Code
A01020102 ASPIRATION FINE NEEDLES AND KITS 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

Category: Diskectomy system, percutaneous, automatic

CytoCut by M.d.l. S.r.l. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Diskectomy system, percutaneous, automatic.

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 76be8c69-9f22-4ce1-a18f-9a63b5f93dbb 61 fields · synced May 21, 2026