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Lettino Selene 2

EUDAMED

Class I (EU MDR)

Ref 1121FModel SERIE NEW PROFESSIONAL

by FISIOTECH srl

Identity

Trade Name
LETTINO SELENE 2 EUDAMED
Device Name
SELENE 2 EUDAMED
Model / Reference
SERIE NEW PROFESSIONAL EUDAMED
1121F EUDAMED

Identifiers

Primary DI / UDI-DI
80505939406504 EUDAMED
Basic UDI-DI
8050593941121FSK EUDAMED
Direct Marketing DI
80505939406504 EUDAMED
EMDN Code
Z12069099 VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER 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

Lettino Selene 2 by FISIOTECH srl — 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
FISIOTECH srl
EUDAMED SRN
IT-MF-000028185

Sources (1)

  • EUDAMED a8a065d8-8490-410f-a4d9-5d25cc63caf9 61 fields · synced Jul 13, 2026