| Primary Device ID | 00887517206138 |
| NIH Device Record Key | 4c6f28f3-5480-4d15-927d-c3f702aa82bf |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 8010050 |
| Company DUNS | 053950783 |
| Company Name | Nuvasive, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 | +1(858)909-1800 |
| RA_UDI@nuvasive.com | |
| Phone | +1(858)909-1800 |
| RA_UDI@nuvasive.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887517206138 [Primary] |
| GWF | STIMULATOR, ELECTRICAL, EVOKED RESPONSE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-26 |
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| 00195377055538 - Nimbus | 2024-05-01 Nimbus Adapter, Large Clamp |
| 00195377055545 - Nimbus | 2024-05-01 Nimbus Adapter, Medium Clamp |
| 00195377055552 - Nimbus | 2024-05-01 Nimbus Adapter, Small Clamp |
| 00195377061232 - Nimbus | 2024-05-01 Nimbus Adapters Tray |