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Culla

EUDAMED

Class I (EU MDR)

Ref CT32003Model CT32003, 332100

by Malvestio Spa

Identity

Device Name
CULLA EUDAMED
Model / Reference
CT32003, 332100 EUDAMED
CT32003 EUDAMED

Identifiers

Primary DI / UDI-DI
08058302602622 EUDAMED
Basic UDI-DI
805830260CULLA9U EUDAMED
Direct Marketing DI
08058302602622 EUDAMED
EMDN Code
V0809 MANUAL CLINICAL CRIBS FOR NEWBORNS 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

Culla by Malvestio Spa — 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

Manufacturer
Malvestio Spa
EUDAMED SRN
IT-MF-000013307

Sources (1)

  • EUDAMED 042f934c-281f-4b03-a7f2-efdaa193cc74 61 fields · synced Jul 13, 2026