Identity
- Trade Name
- Trift EUDAMED
- Device Name
- Trift PTA Balloon Dilatation Catheter EUDAMED
- Model / Reference
- PS35-080060-150 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08720621348498 EUDAMED
- Basic UDI-DI
- 872062130005AK EUDAMED
- EMDN Code
- C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED
Classification
- Device Class
- Class IIa 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
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Category: Peripheral angioplasty balloon catheter, basic
Trift by Cnovate Medical B.V. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Peripheral angioplasty balloon catheter, basic.
- Minerva PTA Balloon Dilatation Catheter — BrosMed Medical Co., Ltd. · Class IIa
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- Senri — KANEKA Corporation · Class IIa
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- ZENFluxion — Zylox-Tonbridge Medical Technology Co., Ltd. · Class III
- Pacific™ Plus — MEDTRONIC, INC. · Class II
- Metacross OTW — KANEKA Corporation · Class IIa
- Armada — Abbott Vascular · Class II
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 872062130005AK | Class IIa | Active |
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Manufacturer
- Manufacturer
- Cnovate Medical B.V.
- EUDAMED SRN
- NL-MF-000006042
Sources (1)
- EUDAMED 1c160b92-1dbc-4a0a-81cc-ef32f428cbe0 61 fields · synced Jun 18, 2026