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Vela

EUDAMED

Class IIa (EU MDR)

Ref 21450040

by Curatia Medical Limited

Identity

Trade Name
Vela EUDAMED
Device Name
Vela OTW PTA Balloon Dilatation Catheter EUDAMED
Model / Reference
21450040 EUDAMED

Identifiers

Primary DI / UDI-DI
06941358014384 EUDAMED
Basic UDI-DI
697022652108FU EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Vela by Curatia Medical Limited — Class IIa — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000015976
Authorised Representative
MedNet EC-REP III GmbH DE-AR-000011191

Sources (1)

  • EUDAMED 81d4ee7a-ea81-42da-ba98-659914be7244 61 fields · synced Oct 7, 2026