No Certificate Found

Snapshot 2026-10-31 · Link to EUDAMED

Bende Previforte (PREVIS)

UDI-DI 08033140280607Basic UDI-DI 803314028M0304010103NZ

Class I · MDR · Previs S.r.l.

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Identification

Model: —
EMDN: M0304010103
Issuing agency: GS1
Device status: active
Sterile: No
Implantable: No
Measuring function: No
Reusable surgical: No

Certificates

No certificate found.

Snapshot 2026-10-31 · Link to EUDAMED

Manufacturer

SRN IT-MF-000017072

IT · Trissino (VI)

manufacturer

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Bende Previmedia (PREVIS) 08033140282878
Bende Previmedia (PREVIS) 08033140282892
Bende Previmedical (PREVIS) 08033140281604
Bende Previmedical (PREVIS) 08033140282861
Bende Previmedical (PREVIS) 08033140281598
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Bende Previmedical (PREVIS) 08033140281581
Bende Previmedical (PREVIS) 08033140281611

Showing 12 of 33 other UDI-DIs.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/bende-previforte-previs-0607 · UDI page: /udi/08033140280607

All devices from Previs S.r.l.

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