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AngioSculpt PTCA RX Scoring Balloon Catheter

EUDAMEDFDA UDI

Class III (EU MDR)

Ref 2200-2006

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 6 mm FDA UDI
Model / Reference
2200-2006 EUDAMEDFDA UDI
Description
2.0 mm x 6 mm FDA UDI

Identifiers

Catalog Number
2200-2006 FDA UDI
Primary DI / UDI-DI
00813132021139 EUDAMEDFDA UDI
Basic UDI-DI
B-00813132021139 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

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

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 — 06 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

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Manufacturer

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

Sources (2)

  • EUDAMED 64f3f36a-9d26-47d2-83a8-bd954d38f46b 61 fields · synced May 30, 2026
  • FDA UDI a3570bc2-c2ef-4eaa-b03b-885b667810bf 38 fields · synced May 30, 2026