Certificate valid

Snapshot 2026-10-12 · Link to EUDAMED

InRo®

UDI-DI 07630033312936Basic UDI-DI 076300333IF_CBLCATHL4

Class III · MDR · Rontis Corporation SA

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Identification

Model: InRo® Family
EMDN: C010401020101
Issuing agency: GS1
Device status: active
Sterile: Yes
Implantable: No
Measuring function: No
Reusable surgical: No

Certificates

44912221174

EU technical documentation assessment · valid

Notified body: TÜV NORD CERT GmbH (0044)

Valid from 2024-03-15 · Expiry 2029-03-14

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

Rontis Corporation SA

SRN CH-MF-000031411

CH · Zug

manufacturer

Authorised representative: RONTIS HELLAS MEDICAL AND PHARMACEUTICAL PRODUCTS S.A. (GR-AR-000023077)

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InRo® 07630033313452
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Showing 12 of 58 other UDI-DIs.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/inro-nc-non-compliant-coronary-balloon-catheter-2-0mmx30mm-2936 · UDI page: /udi/07630033312936

All devices from Rontis Corporation SA

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