FDA UDI Not in Commercial Distribution 🇺🇸 United States

AngioSculpt®

DI: M3702039201015 · Model: 2039-2010-A · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AngioSculpt®
Primary DI
M3702039201015
Version / Model
2039-2010-A
Catalog Number
2039-2010
Company Name
Spectranetics Corporation
Labeler DUNS
151047370
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2023-08-02
Public Version Status
Update
Public Device Record Key
77f5c775-25a5-46af-bbdb-1cba87677424
Distribution End Date
2020-02-20

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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
PNO Catheter, Percutaneous, Cutting/Scoring

GMDN Terms

Code Name
17184 Peripheral angioplasty balloon catheter, basic

Identifiers

Type ID
Primary M3702039201015

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10 Millimeter
Outer Diameter 2.0 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 140 Degrees Fahrenheit