Primary Device ID | 00670082000061 |
NIH Device Record Key | 133deb4e-4b92-43e6-aa57-e4264d6c2352 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BrightMatter Guide |
Version Model Number | SYN-0026 |
Company DUNS | 203061833 |
Company Name | Synaptive Medical Inc |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 | 00670082000061 [Primary] |
HAW | Neurological Stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
00670082000603 - Modus IR | 2024-04-10 Surgical Exoscope Fluorescence Filter |
10670082000495 - Evry | 2023-10-24 |
00670082000511 - Modus Plan | 2023-10-18 |
00670082000566 - Modus X | 2023-03-14 Robotic Exoscope |
00670082000573 - Modus X | 2023-03-14 Robotic Exoscope |
00670082000580 - Modus Blue | 2023-03-14 Robotic Exoscope Fluorescence Filter |
00670082000085 - BrightMatter Plan | 2019-08-16 |
00670082000160 - BrightMatter Plan | 2019-08-16 |