| Primary Device ID | 00850359007059 |
| NIH Device Record Key | 8eaad903-7dc9-4c8f-88a6-764129263809 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MRI Interventions |
| Version Model Number | NGS-HX-M6 |
| Catalog Number | NGS-HX-M6 |
| Company DUNS | 959181160 |
| Company Name | MRI INTERVENTIONS, INC. |
| 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 | false |
| 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 |
| Phone | 949-900-6833 |
| info@mriinterventions.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850359007059 [Primary] |
| ORR | Neurological Stereotaxic Instrument, Real-Time Intraoperative Mri |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-02-07 |
| 00850359007059 | Hex Key, 5 mm, MR Conditional |
| 00850359007058 | M6 Bolt Drive with T Handle. MR Safe |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MRI INTERVENTIONS 85324070 4239410 Live/Registered |
MRI Interventions, Inc. 2011-05-18 |
![]() MRI INTERVENTIONS 85324064 4358485 Live/Registered |
MRI Interventions, Inc. 2011-05-18 |