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AngioSculpt PTCA RX Scoring Balloon Catheter
EUDAMEDFDA UDIClass III (EU MDR)
Ref 2200-3506
Identity
- Trade Name
- AngioSculpt PTCA RX Scoring Balloon Catheter EUDAMEDFDA UDI
- Generic Name
- Coronary angioplasty balloon catheter, cutting/scoring FDA UDI
- Device Name
- AngioSculpt PTCA RX Scoring Balloon Catheter EUDAMED3.5 mm x 6 mm FDA UDI
- Model / Reference
- 2200-3506 EUDAMEDFDA UDI
- Description
- 3.5 mm x 6 mm FDA UDI
Identifiers
- Catalog Number
- 2200-3506 FDA UDI
- Primary DI / UDI-DI
- 00813132021221 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00813132021221 EUDAMED
- PMA Number
- P050018 FDA UDI
- FDA Product Code
- NWX FDA UDI
- EMDN Code
- C010401020101 PTCA BALLOON DILATION CATHETERS EUDAMED
- GMDN Term
- Coronary angioplasty balloon catheter, cutting/scoring FDA UDI
Classification
- Device Class
- Class III EUDAMEDFDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Balloon Diameter — 3.5 Millimeter FDA UDIBalloon Length — 06 Millimeter FDA UDI
AngioSculpt PTCA RX Scoring Balloon Catheter by Spectranetics Corporation — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00813132021221 | Class III | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Spectranetics Corporation
- EUDAMED SRN
- US-MF-000023203
- Authorised Representative
- Spectranetics International B.V. NL-AR-000001484
Sources (2)
- EUDAMED 03bf973b-7405-492e-8323-06f6053dba6a 61 fields · synced May 31, 2026
- FDA UDI b63a18aa-f542-4755-8af0-af28df70bcff 38 fields · synced May 29, 2026