FDA UDI In Commercial Distribution 🇺🇸 United States

Precision ™

DI: 08714729767640 · Model: 5093144-001 · BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Precision ™
Primary DI
08714729767640
Version / Model
5093144-001
Company Name
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
Labeler DUNS
824951958
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-09
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
723d2f3a-9422-4005-bc04-c71bb10fd4d3

Device Description

Cable, USB-Serial

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LGW STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

GMDN Terms

Code Name
36007 Analgesic spinal cord electrical stimulation system

Identifiers

Type ID
Primary 08714729767640

Premarket Submissions

Submission Number Supplement Number
P030017 000