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Europa Ultra CTO - Chronic Total Occlusion Coronary Balloon Catheter Rx 1.0mmx1…

EUDAMED

Class III (EU MDR)

Ref EC10/16Model Europa Ultra™ Family

by Rontis Corporation SA

Identity

Trade Name
Europa Ultra™ EUDAMED
Device Name
Europa Ultra CTO - Chronic Total Occlusion Coronary Balloon Catheter Rx 1.0mmx16mm EUDAMED
Europa Ultra Coronary Balloon Catheter EUDAMED
Model / Reference
EC10/16 EUDAMED
Europa Ultra™ Family EUDAMED

Identifiers

Primary DI / UDI-DI
07630033300483 EUDAMED
Basic UDI-DI
B-07630033300483 EUDAMED
076300333EF_CBLCATHGG EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Cyprus EUDAMED

Clinical & Handling

Sterile

Yes

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

Category: Coronary angioplasty balloon catheter, cutting/scoring

Europa Ultra CTO - Chronic Total Occlusion Coronary Balloon Catheter Rx 1.0mmx1… by Rontis Corporation SA — Class III — MDR, MDD — listed in EUDAMED

Similar devices

Also classified as Coronary angioplasty balloon catheter, cutting/scoring.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CH-MF-000031411
Authorised Representative
RONTIS HELLAS MEDICAL AND PHARMACEUTICAL PRODUCTS S.A. GR-AR-000023077

Sources (2)

  • EUDAMED f9249c2c-ce3e-43c3-8b0e-bf8887d0fcc3 61 fields · synced Oct 6, 2026
  • EUDAMED fe3652d6-a418-44d7-933c-1e2794b23417 61 fields · synced May 18, 2026