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Bassinettes

EUDAMED

Class I (EU MDR)

Ref M620030Model Bassinettes

by Titanox S.r.l.

Identity

Device Name
Bassinettes EUDAMED
Model / Reference
Bassinettes EUDAMED
M620030 EUDAMED

Identifiers

Primary DI / UDI-DI
08059304703102 EUDAMED
Basic UDI-DI
805930470M01CULZQ 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

Bassinettes by Titanox 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

Manufacturer
Titanox S.r.l.
EUDAMED SRN
IT-MF-000020325

Sources (1)

  • EUDAMED 68454c00-e028-449d-9881-b7fe724ab410 61 fields · synced Jul 27, 2026