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Stellarex 0.035" OTW Drug-coated Angioplasty Balloon

EUDAMED

Class III (EU MDR)

Ref A35SX050150080

by Spectranetics Corporation

Identity

Trade Name
Stellarex 0.035" OTW Drug-coated Angioplasty Balloon EUDAMED
Device Name
Stellarex .035 OTW Drug-coated Angioplas EUDAMED
Stellarex 0.035" OTW Drug-coated Angioplasty Balloon EUDAMED
Model / Reference
A35SX050150080 EUDAMED

Identifiers

Primary DI / UDI-DI
00813132027018 EUDAMED
Basic UDI-DI
B-00813132027018 EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Netherlands 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

Yes

EUDAMED

Category: Peripheral angioplasty balloon catheter, basic

Stellarex 0.035" OTW Drug-coated Angioplasty Balloon by Spectranetics Corporation — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
US-MF-000020669
Authorised Representative
Spectranetics International B.V. NL-AR-000001484

Sources (2)

  • EUDAMED 8228c095-e069-4494-971e-c1122aa4d365 61 fields · synced Oct 6, 2026
  • EUDAMED f6e85527-31a0-4d6a-a208-a58559fc29c2 61 fields · synced Jul 28, 2026