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Letti LYTUS tre sezioni

EUDAMED

Class I (EU MDR)

Ref MI310B

by Moretti Spa

Identity

Device Name
Letti LYTUS tre sezioni EUDAMED
Model / Reference
MI310B EUDAMED

Identifiers

Primary DI / UDI-DI
08052879646355 EUDAMED
Basic UDI-DI
805287964202301Q9 EUDAMED
Direct Marketing DI
08052879646355 EUDAMED
EMDN Code
V080603 TREATMENT, DIAGNOSIS AND MONITORING 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

Letti LYTUS tre sezioni by Moretti 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
Moretti Spa
EUDAMED SRN
IT-MF-000005980

Sources (1)

  • EUDAMED c6a9ee59-9543-421c-999a-c46fe199e8ea 61 fields · synced Jun 17, 2026