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Europa Ultra NC - Non-Compliant Coronary Balloon Catheter 3.5mmx15mm

EUDAMED

Class III (EU MDR)

Ref EN35/15Model Europa Ultra™ Family

by Rontis Corporation SA

Identity

Trade Name
Europa Ultra™ EUDAMED
Device Name
Europa Ultra NC - Non-Compliant Coronary Balloon Catheter 3.5mmx15mm EUDAMED
Europa Ultra Coronary Balloon Catheter EUDAMED
Model / Reference
EN35/15 EUDAMED
Europa Ultra™ Family EUDAMED

Identifiers

Primary DI / UDI-DI
07630033300926 EUDAMED
Basic UDI-DI
B-07630033300926 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 NC - Non-Compliant Coronary Balloon Catheter 3.5mmx15mm 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 cfbbdc17-99e2-4db3-8fa3-5abd24d489cd 61 fields · synced Oct 6, 2026
  • EUDAMED 8d2bba58-7676-4b84-852d-a304006b5ccd 61 fields · synced May 16, 2026