Bende Elastiche

by BENEFIS S.r.l. 17 variants

Ref E1840412

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number805299200BEBEVM0304EU Basic UDI-DI 08052992012617UDI-DI	Date6 Nov 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference: E1840412

Primary DI / UDI-DI: 08052992012617
Basic UDI-DI: 805299200BEBEVM0304EU
EMDN code: M0304010302 Elastic compression bandages, adhesive, medium extensibility (70-140%)

Device class: Class I
EU registration type: Standard device
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: IT-MF-000022530

Other devices from BENEFIS S.r.l.

Monouso Standard

Class I
Bende Elastiche

Class I
Cerotti

Class I
Mascherine

Class I
Monouso Standard

Class I
Cerotti

Class I

See all devices from BENEFIS S.r.l. →

Properties

Other properties (14)

Supplied sterile: No
Sterilise before use: No
Implantable: No
Reusable: No
Contains latex: No
Reprocessed single-use device: No
Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
Incorporates a substance derived from human blood or plasma: No
Contains human tissues or cells: No
Contains animal tissues or cells: No
Contains endocrine-disrupting substances: No
Administering medicine: No
Measuring function: No
Incorporates a medicinal substance: No