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Lettino Titan 2

EUDAMED

Class I (EU MDR)

Ref 1113EModel SERIE BOBATH

by FISIOTECH srl

Identity

Trade Name
LETTINO TITAN 2 EUDAMED
Device Name
TITAN 2 EUDAMED
Model / Reference
SERIE BOBATH EUDAMED
1113E EUDAMED

Identifiers

Primary DI / UDI-DI
80505939411072 EUDAMED
Basic UDI-DI
8050593941113ESJ EUDAMED
Direct Marketing DI
80505939411072 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 Titan 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 3b331cc0-3d27-4750-8a97-03da026cdb74 61 fields · synced Jun 18, 2026