Primary Device ID | 00850376007895 |
NIH Device Record Key | 19c101cb-dbe8-4d1a-aba1-55cd3a101665 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ClearPoint Array |
Version Model Number | CPA-WRK-02 |
Catalog Number | CPA-WRK-02 |
Company DUNS | 959181160 |
Company Name | CLEARPOINT NEURO, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | 00850376007895 [Primary] |
HAW | Neurological Stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-11-06 |
Device Publish Date | 2023-10-27 |
00850359007744 | ClearPoint Lite Software |
00850376007659 | ClearPoint Array Software Version 1.1 |
00850376007895 | ClearPoint Array v1.2.x Neuro Workstation |
00850376007871 | ClearPoint Array Software Version 1.2 |