FDA UDI In Commercial Distribution 🇺🇸 United States

Stellarex

DI: 00813132023218 · Model: AB35SX050080135 · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Stellarex
Primary DI
00813132023218
Version / Model
AB35SX050080135
Catalog Number
AB35SX050080135
Company Name
Spectranetics Corporation
Labeler DUNS
151047370
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-27
Public Version
10
Public Version Date
2023-08-14
Public Version Status
Update
Public Device Record Key
3f33fcb7-a94b-43f7-be1e-7adc68ee634d

Device Description

Stellarex 0.035 OTW Drug-coated Angioplasty Balloon (5mm x 80mm) x 135cm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
ONU Drug-Eluting Peripheral Transluminal Angioplasty Catheter

GMDN Terms

Code Name
62551 Peripheral angioplasty balloon catheter, drug-coated

Identifiers

Type ID
Primary 00813132023218

Customer Contacts

Device Sizes

Type Value Unit Text
Balloon Diameter 5 Millimeter
Balloon Length 80 Millimeter
Catheter Length 135 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep dry