← Back to catalogue

AngioSculpt PTCA RX Scoring Balloon Catheter

EUDAMEDFDA UDI

Class III (EU MDR)

Ref 2200-2015

by Spectranetics Corporation

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 EUDAMED
2.0 mm x 15 mm FDA UDI
Model / Reference
2200-2015 EUDAMEDFDA UDI
Description
2.0 mm x 15 mm FDA UDI

Identifiers

Catalog Number
2200-2015 FDA UDI
Primary DI / UDI-DI
00813132021153 EUDAMEDFDA UDI
Basic UDI-DI
B-00813132021153 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 — 2.0 Millimeter FDA UDI
Balloon Length — 15 Millimeter FDA UDI

Category: Coronary angioplasty balloon catheter, cutting/scoring

AngioSculpt PTCA RX Scoring Balloon Catheter by Spectranetics Corporation — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Coronary angioplasty balloon catheter, cutting/scoring.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000023203
Authorised Representative
Spectranetics International B.V. NL-AR-000001484

Sources (2)

  • EUDAMED e0adfbae-edc7-4738-ab30-4e5f796fd6f0 61 fields · synced Oct 1, 2026
  • FDA UDI 5b1b4e31-b137-43b3-a3c0-dbbc7d736aa6 38 fields · synced May 30, 2026