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Atlante

EUDAMED

Class I (EU MDR)

Ref 378300SModel 378300, 378300S

by Malvestio Spa

Identity

Trade Name
ATLANTE EUDAMED
Device Name
ATLANTE EUDAMED
Model / Reference
378300, 378300S EUDAMED
378300S EUDAMED

Identifiers

Primary DI / UDI-DI
08058302603179 EUDAMED
Basic UDI-DI
805830260ATLANTENBBL EUDAMED
Direct Marketing DI
08058302603179 EUDAMED
EMDN Code
V08060102 INTENSIVE CARE OR RESUSCITATION ELECTRIC MEDICAL BEDS 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

Atlante 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 869b0e09-04b3-4ecc-b36a-d43d0463ed53 61 fields · synced Jun 19, 2026