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Lettino Iride

EUDAMED

Class I (EU MDR)

Ref 1111GModel SERIE PROFESSIONAL

by FISIOTECH srl

Identity

Trade Name
LETTINO IRIDE EUDAMED
Device Name
IRIDE EUDAMED
Model / Reference
SERIE PROFESSIONAL EUDAMED
1111G EUDAMED

Identifiers

Primary DI / UDI-DI
80505939404906 EUDAMED
80505939404838 EUDAMED
Basic UDI-DI
8050593941111GSG EUDAMED
Direct Marketing DI
80505939404906 EUDAMED
80505939404838 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 Iride 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 (2)

  • EUDAMED cc37e4dd-e628-4150-b08a-99a021edfdb7 61 fields · synced Jul 9, 2026
  • EUDAMED a644ddd1-6617-4ea8-b722-a21dff054903 61 fields · synced May 18, 2026