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Benda Elastica

EUDAMED

Class I (EU MDR)

Ref BENELA1DPModel BENDA ELASTICA

by Bericah S.p.A.

Identity

Trade Name
BENDA ELASTICA EUDAMED
Device Name
BENDA ELASTICA EUDAMED
Model / Reference
BENDA ELASTICA EUDAMED
BENELA1DP EUDAMED

Identifiers

Primary DI / UDI-DI
08024151816848 EUDAMED
Basic UDI-DI
8024151BENELN9 EUDAMED
Direct Marketing DI
08024151816848 EUDAMED
EMDN Code
M0304010102 ELASTIC COMPRESSION BANDAGES, NON-ADHESIVE, MEDIUM EXTENSIBILITY (70-140%) 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 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 0e7620b5-a065-402d-9413-9fe20de885b7 61 fields · synced Jun 18, 2026