| Primary Device ID | 00763000047375 |
| NIH Device Record Key | 3cdf9d59-ef94-4a3c-b911-a36918cac3a8 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 9733752R |
| Company DUNS | 835233107 |
| Company Name | MEDTRONIC NAVIGATION, 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000047375 [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 | 2019-06-04 |
| Device Publish Date | 2019-05-27 |
| 00763000738419 - AxiEM™ | 2025-04-07 TRACKER 9734887 NON-INVASIVE PATIENT |
| 00763000738426 - AxiEM™ | 2025-04-07 PATIENT TRACKER 9734887XOM NON-INVASIVE |
| 00763000738457 - AxiEM™ | 2025-04-07 INSTRUMENT TRACKER 9733533XOM ENT 1PK |
| 00763000738471 - AxiEM™ | 2025-04-07 PATIENT TRACKER 9733534XOM ENT 1PK |
| 00763000738495 - Aquamantys™ | 2025-04-01 AQUAMANTYS 9.5 XL BIPOLAR SEALER DEVICE |
| 00763000738501 - Aquamantys™ | 2025-04-01 AQM 6.0 BIPOLAR SEALER UNIT |
| 00763000738556 - Aquamantys™ | 2025-04-01 AQUAMANTYS 2.3 BIPOLAR SEALER UNIT |
| 00763000972318 - N/A | 2025-03-31 EMITTER 9733752R FLAT CALIBRATED |