Primary Device ID | 08503590070580 |
NIH Device Record Key | 509d4f5f-f171-42bc-87c9-512cebc967ad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MRI Interventions |
Version Model Number | NGS-BD-M6 |
Catalog Number | NGS-BD-M6 |
Company DUNS | 959181160 |
Company Name | CLEARPOINT NEURO, 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 | 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 | 08503590070580 [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 | 4 |
Public Version Date | 2020-03-12 |
Device Publish Date | 2017-02-07 |
08503590070597 | Hex Key, 5 mm, MR Conditional |
08503590070580 | M6 Bolt Drive with T Handle. MR Safe |
00850359007591 | Hex Key, 5 mm, MR Conditional |
00850359007584 | 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 |