Primary Device ID | 08714729991380 |
NIH Device Record Key | 2492bc44-48fa-473d-bc77-010aa3abae29 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bionic Navigator™ |
Version Model Number | SC-7101-102-W10 |
Company DUNS | 824951958 |
Company Name | BOSTON SCIENTIFIC NEUROMODULATION CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729991380 [Primary] |
LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-02-10 |
Device Publish Date | 2020-01-31 |
08714729991380 | 1.2 Installer |
08714729991328 | 2.04 Installer |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BIONIC NAVIGATOR 78232729 3036464 Live/Registered |
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION 2003-04-01 |