Primary Device ID | 08714729984443 |
NIH Device Record Key | df7ff149-7874-4241-870e-c82432de68fe |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vercise Gevia™ |
Version Model Number | DB-1200-S |
Company DUNS | 824951958 |
Company Name | BOSTON SCIENTIFIC NEUROMODULATION CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
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 | 08714729984443 [Primary] |
NHL | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2021-11-03 |
Device Publish Date | 2019-01-15 |
08714729966333 - Vercise™ Cartesia™ X | 2024-12-23 Directional Lead Kit, 16 Contact, 30cm |
08714729966340 - Vercise™ Cartesia™ X | 2024-12-23 Directional Lead Kit, 16 Contact, 45cm |
08714729966357 - Vercise™ Cartesia™ HX | 2024-12-23 Directional Lead Kit, 16 Contact, 30cm |
08714729966364 - Vercise™ Cartesia™ HX | 2024-12-23 Directional Lead Kit, 16 Contact, 45cm |
08714729966371 - NA | 2024-12-23 Lead Extension Kit, 2x8 Contact, 55cm |
08714729966388 - NA | 2024-12-23 Lead Extension Kit, 2x8 Contact, 95cm |
08714729966395 - NA | 2024-12-23 16 Contact Lead Extension Kit, 55 cm |
08714729966401 - NA | 2024-12-23 16 Contact Lead Extension Kit, 95 cm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VERCISE GEVIA 87014694 not registered Live/Pending |
Boston Scientific Neuromodulation Corporation 2016-04-26 |