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P0603em

EUDAMED

Class IIa (EU MDR)

Ref P0603EMModel P0603EM F400

by FLAEM NUOVA SpA

Identity

Model / Reference
P0603EM F400 EUDAMED
P0603EM EUDAMED

Identifiers

Primary DI / UDI-DI
08018294015794 EUDAMED
Basic UDI-DI
8018294P0603EM_F400JJ EUDAMED
Direct Marketing DI
08018294015794 EUDAMED
EMDN Code
Z12159002 AEROSOL EQUIPMENT 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

P0603em by FLAEM NUOVA SpA — 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

Manufacturer
FLAEM NUOVA SpA
EUDAMED SRN
IT-MF-000007769

Sources (1)

  • EUDAMED 3ab9b3c2-ed7f-4cd5-a15d-3fa051918059 61 fields · synced Jul 24, 2026