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Europa Ultra NC - Non-Compliant Coronary Balloon Catheter 3.0mmx15mm

EUDAMED

Class III (EU MDR)

Ref EN30/15Model Europa Ultra™ Family

by Rontis Corporation SA

Identity

Trade Name
Europa Ultra™ EUDAMED
Device Name
Europa Ultra NC - Non-Compliant Coronary Balloon Catheter 3.0mmx15mm EUDAMED
Europa Ultra Coronary Balloon Catheter EUDAMED
Model / Reference
EN30/15 EUDAMED
Europa Ultra™ Family EUDAMED

Identifiers

Primary DI / UDI-DI
07630033300872 EUDAMED
Basic UDI-DI
B-07630033300872 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

Europa Ultra NC - Non-Compliant Coronary Balloon Catheter 3.0mmx15mm 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 f58140e3-05d6-4afa-9a3f-394a4427af9d 61 fields · synced Oct 7, 2026
  • EUDAMED 1f9d3439-5c12-43ad-832b-22fe85a368f5 61 fields · synced May 18, 2026