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Europa Ultra - Semi-Compliant Coronary Balloon Catheter 5.0mmx30mm

EUDAMED

Class III (EU MDR)

Ref EL50/30Model Europa Ultra™ Family

by Rontis Corporation SA

Identity

Trade Name
Europa Ultra™ EUDAMED
Device Name
Europa Ultra - Semi-Compliant Coronary Balloon Catheter 5.0mmx30mm EUDAMED
Europa Ultra Coronary Balloon Catheter EUDAMED
Model / Reference
EL50/30 EUDAMED
Europa Ultra™ Family EUDAMED

Identifiers

Primary DI / UDI-DI
07630033300452 EUDAMED
Basic UDI-DI
B-07630033300452 EUDAMED
076300333EF_CBLCATHGG EUDAMED
EMDN Code
C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Greece 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 - Semi-Compliant Coronary Balloon Catheter 5.0mmx30mm 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 31626c42-be27-4266-978c-474535034289 61 fields · synced Jun 18, 2026
  • EUDAMED bb698492-d667-4f9a-ad91-14105699453b 61 fields · synced May 18, 2026