FDA UDI In Commercial Distribution 🇺🇸 United States

Bridge™ Occlusion Balloon

DI: 00813132023263 · Model: 590-001 · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bridge™ Occlusion Balloon
Primary DI
00813132023263
Version / Model
590-001
Catalog Number
590-001
Company Name
Spectranetics Corporation
Labeler DUNS
151047370
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-02-25
Public Version
6
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
85577e2c-22d8-486c-bec5-e9f1bc8ae8d3

Device Description

Bridge Occlusion Catheter - 80 mm Length Balloon

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
MJN Catheter, Intravascular Occluding, Temporary

GMDN Terms

Code Name
32584 Intravascular occluding balloon catheter, image-guided

Identifiers

Type ID
Primary 00813132023263

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K153530 000

Device Sizes

Type Value Unit Text
Length 90 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 140 Degrees Fahrenheit