| Primary Device ID | 07290014954489 |
| NIH Device Record Key | e4a7f2e2-c555-4ec0-b506-f6130396ef48 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NeuroProbe |
| Version Model Number | Non-shielded |
| Catalog Number | STR-34685Z-00 |
| Company DUNS | 531856466 |
| Company Name | ALPHA OMEGA ENGINEERING CO. LTD. |
| 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 | 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 | 8779196288 |
| m.andrea@alphaomega-eng.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290014954489 [Primary] |
| GS1 | 17290014954486 [Package] Package: carton [10 Units] In Commercial Distribution |
| GZL | Electrode, Depth |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-22 |
| Device Publish Date | 2016-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEUROPROBE 73139404 1114455 Dead/Expired |
ELMED INCORPORATED 1977-08-30 |