FDA UDI In Commercial Distribution 🇺🇸 United States

FINELINE® II EZ Sterox

DI: 00802526264993 · Model: 4470 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FINELINE® II EZ Sterox
Primary DI
00802526264993
Version / Model
4470
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
106295384
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
6
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
8a787e83-0d09-41f0-822c-0b1dda0f3895

Device Description

Sterox Bipolar IS-1 Atrial/Ventricular

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DTB permanent pacemaker Electrode

GMDN Terms

Code Name
35223 Endocardial pacing lead

Identifiers

Type ID
Primary 00802526264993

Premarket Submissions

Submission Number Supplement Number
P960004 022
P960004 039
P960004 041
P960004 042
P960004 059
P960004 060
P960004 078
P960004 081
P960004 085
P960004 088

Device Sizes

Type Value Unit Text
Device Size Text, specify 52 cm Length