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Penta30epa

EUDAMED

Class I (EU MDR)

Ref PENTA30E

by RIMSA P. LONGONI S.r.l.

Identity

Trade Name
PENTA30EPA EUDAMED
Device Name
LAMPADE SCIALITICHE PER USO CHIRURGICO E PER LA DIAGNOSI EUDAMED
Model / Reference
PENTA30E EUDAMED

Identifiers

Primary DI / UDI-DI
B880PENTA30E0 EUDAMED
Basic UDI-DI
++B880LUMINAIREPM EUDAMED
Direct Marketing DI
B880PENTA30E0 EUDAMED
EMDN Code
Z12010701,Z12010702 EUDAMED

Classification

Device Class
Class I 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

Penta30epa by RIMSA P. LONGONI S.r.l. — Class I — 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-000009224

Sources (1)

  • EUDAMED d851fdf1-df77-4408-b706-4d5a05c9fdf7 61 fields · synced Jul 31, 2026