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Europa Ultra CTO - Chronic Total Occlusion Coronary Balloon Catheter Rx 1.5mmx2…

EUDAMED

Class III (EU MDR)

Ref EC15/20Model 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 1.5mmx20mm EUDAMED
Europa Ultra Coronary Balloon Catheter EUDAMED
Model / Reference
EC15/20 EUDAMED
Europa Ultra™ Family EUDAMED

Identifiers

Primary DI / UDI-DI
07630033300551 EUDAMED
Basic UDI-DI
B-07630033300551 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

Europa Ultra CTO - Chronic Total Occlusion Coronary Balloon Catheter Rx 1.5mmx2… by Rontis Corporation SA — Class III — MDR, MDD — listed in EUDAMED

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 bca3d0c8-d15c-4276-b12b-79e1408996ae 61 fields · synced Jun 19, 2026
  • EUDAMED d4f6add7-b7d4-43a3-a818-a47c22f0b084 61 fields · synced May 17, 2026