| Primary Device ID | 07290014954281 |
| NIH Device Record Key | 5174487c-649b-4945-aaa6-17d71ec16724 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Neuro Omega Input Cable |
| Version Model Number | 3 channels MER only |
| Catalog Number | STR-000666-33 |
| 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 | 07290014954281 [Primary] |
| GS1 | 17290014954288 [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 | 4 |
| Public Version Date | 2019-11-22 |
| Device Publish Date | 2016-09-24 |
| 07290014954304 | 5 channels MER only |
| 07290014954298 | 4 channels MER only |
| 07290014954281 | 3 channels MER only |
| 07290014954274 | 2 channels MER only |
| 07290014954267 | 1 channel MER only |
| 07290014954250 | 5 channels |
| 17290014954240 | 4 channels |
| 17290014954233 | 3 channels |
| 17290014954226 | 2 channels |
| 17290014954219 | 1 channel |