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Uniko Pz

EUDAMED

Class IIa (EU MDR)

Ref MiniUNIKO G

by Mariotti & C. S.r.l.

Identity

Trade Name
Mini UNIKO G EUDAMED
Device Name
UNIKO PZ EUDAMED
Model / Reference
MiniUNIKO G EUDAMED

Identifiers

Primary DI / UDI-DI
08056746330323 EUDAMED
Basic UDI-DI
805674633SURDEVTL EUDAMED
Direct Marketing DI
08056746330323 EUDAMED
EMDN Code
Z12139004 PODOLOGICAL TREATMENT UNITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

Uniko Pz by Mariotti & C. S.r.l. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IT-MF-000035061

Sources (2)

  • EUDAMED f61f3214-742b-4dd3-8015-22def0f5237a 61 fields · synced Jun 19, 2026
  • EUDAMED 54cdb8f4-29c6-4acd-ade3-18356f9eaa5d 61 fields · synced Jun 19, 2026