| Primary Device ID | 20613994747888 |
| NIH Device Record Key | 800f6325-867d-4116-b613-c2825ecf4c33 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | SR-10 |
| Company DUNS | 796986144 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 3 |
| 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 | false |
| 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 |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994747884 [Unit of Use] |
| GS1 | 20613994747888 [Primary] |
| HAW | Neurological stereotaxic Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-11-18 |
| 00199150025381 - NA | 2025-06-27 CUSTOM PACK BB11P25R3 VCH CENT V A |
| 20199150025521 - NA | 2025-06-27 CUSTOM PACK BB9G37R2 5PK L VD AC |
| 00199150026326 - NA | 2025-06-27 CUSTOM PACK BB11Z33R8 ALINA CPB |
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| 00199150026692 - NA | 2025-06-27 CUSTOM PACK BB8R73R14 NH ADULT PACK |
| 00199150026715 - NA | 2025-06-27 CUSTOM PACK BB6M71R12 CP PRIME |
| 00199150026746 - NA | 2025-06-27 CUSTOM PACK BB7A25R12 PED |
| 00199150026753 - NA | 2025-06-27 CUSTOM PACK BB12E34R4 SUPPORT PACK |