FDA UDI In Commercial Distribution 🇺🇸 United States

Bridge

DI: 00813132024840 · Model: 590-001 · Spectranetics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bridge
Primary DI
00813132024840
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
2017-10-19
Public Version
7
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
37171913-f932-4619-a22b-12c532de0c6b

Device Description

Bridge Occlusion 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
MJN Catheter, Intravascular Occluding, Temporary

GMDN Terms

Code Name
32584 Intravascular occluding balloon catheter, image-guided

Identifiers

Type ID
Primary 00813132024840

Customer Contacts

Device Sizes

Type Value Unit Text
Length 90 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry