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Benda Elastica Fredda

EUDAMED

Class I (EU MDR)

Ref BENELAFR1DPModel BENDA ELASTICA

by Bericah S.p.A.

Identity

Trade Name
BENDA ELASTICA FREDDA EUDAMED
Device Name
BENDA ELASTICA EUDAMED
Model / Reference
BENDA ELASTICA EUDAMED
BENELAFR1DP EUDAMED

Identifiers

Primary DI / UDI-DI
08024151818040 EUDAMED
Basic UDI-DI
8024151BENELN9 EUDAMED
Direct Marketing DI
08024151818040 EUDAMED
EMDN Code
M03040199 ELASTIC COMPRESSION BANDAGES - 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

Benda Elastica Fredda by Bericah S.p.A. — 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
Bericah S.p.A.
EUDAMED SRN
IT-MF-000007397

Sources (1)

  • EUDAMED d6c8649c-68fc-4b08-aa73-9bf8446963fc 61 fields · synced Jul 8, 2026