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iVascular xperience pro
EUDAMEDClass III (EU MDR)
Ref BCPR14N150300030Model xperience pro
Identity
- Trade Name
- iVascular xperience pro EUDAMED
- Device Name
- iVascular xperience pro EUDAMED
- Model / Reference
- xperience pro EUDAMEDBCPR14N150300030 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08435387313887 EUDAMED
- Basic UDI-DI
- 84353873xperiencepro2U EUDAMED
- Direct Marketing DI
- 08435387313887 EUDAMED
- EMDN Code
- C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Spain 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
iVascular xperience pro by Life Vascular Devices Biotech, S.L. — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Peripheral angioplasty balloon catheter, basic.
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- 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 | 84353873xperiencepro2U | Class III | Active |
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Manufacturer
- Manufacturer
- Life Vascular Devices Biotech, S.L.
- EUDAMED SRN
- ES-MF-000019783
Sources (1)
- EUDAMED aa658008-f8ad-4045-a715-b773c7526136 61 fields · synced Aug 1, 2026