| Primary Device ID | 00873263003442 |
| NIH Device Record Key | 8b1d640b-7b21-4936-a953-2304466a821d |
| Commercial Distribution Discontinuation | 2019-06-24 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | microTargeting™ Platform NeuroBlate® Adaptor Kit |
| Version Model Number | 66-WP-NB-00344 |
| Catalog Number | 66-WP-NB |
| Company DUNS | 108179458 |
| Company Name | FHC, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | true |
| 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 |
| Phone | +1(800)326-2905 |
| fhcinc@fh-co.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00873263003442 [Primary] |
| HAW | Neurological stereotaxic Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00873263003442]
Ethylene Oxide;Hydrogen Peroxide;Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-06-24 |
| Device Publish Date | 2016-09-17 |
| 00873263003442 | microTargeting Platform NeuroBlate Adaptor Kit, nonsterile, for use with STarFix Surgical Kit an |
| 00873263006016 | microTargeting Platform NeuroBlate Adaptor Kit, nonsterile, for use with STarFix Surgical Kit an |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MICROTARGETING 78392262 not registered Dead/Abandoned |
TargetPoint Consulting, Inc 2004-03-29 |
![]() MICROTARGETING 76709829 4259360 Dead/Cancelled |
Siren Interactive Corp. 2011-11-23 |
![]() MICROTARGETING 74600530 1921303 Dead/Cancelled |
MBV, INC. 1994-11-18 |