FDA UDI In Commercial Distribution 🇺🇸 United States

AngioSculpt

DI: 00813132021283 · Model: 2039-3020 · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AngioSculpt
Primary DI
00813132021283
Version / Model
2039-3020
Catalog Number
2039-3020
Company Name
Spectranetics Corporation
Labeler DUNS
151047370
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
8
Public Version Date
2023-08-14
Public Version Status
Update
Public Device Record Key
3ac7fbd5-c444-41df-9a46-c68fc1ef134c

Device Description

AngioSculpt PTA Scoring Balloon Catheter

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PNO Catheter, Percutaneous, Cutting/Scoring

GMDN Terms

Code Name
17184 Peripheral angioplasty balloon catheter, basic

Identifiers

Type ID
Primary 00813132021283

Customer Contacts

Device Sizes

Type Value Unit Text
Balloon Length 20 Millimeter
Balloon Diameter 3.0 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry