FDA UDI In Commercial Distribution 🇺🇸 United States

AngioSculpt®PTCA Scoring Balloon Catheter

DI: 00813132021092 · Model: 2027-3020 · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AngioSculpt®PTCA Scoring Balloon Catheter
Primary DI
00813132021092
Version / Model
2027-3020
Catalog Number
2027-3020
Company Name
Spectranetics Corporation
Labeler DUNS
151047370
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-03-09
Public Version
7
Public Version Date
2021-10-26
Public Version Status
Update
Public Device Record Key
4571cd54-3d94-4db3-8792-32ab87a82be3

Device Description

AngioSculpt® PTCA 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
NWX Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/Scoring

GMDN Terms

Code Name
44088 Coronary angioplasty balloon catheter, cutting/scoring

Identifiers

Type ID
Primary 00813132021092

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 3.0 Millimeter
Length 20 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep Dry
Type
Storage Environment Temperature
Temperature Range
– 140 Degrees Fahrenheit