| 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 |
| 00199150033966 - NA | 2025-08-04 CUSTOM PACK BB10N41R3 SUPPORT SM |
| 00199150034017 - NA | 2025-08-04 CUSTOM PACK BB9P05R5 316/14 |
| 20199150034172 - NA | 2025-08-04 CUSTOM PACK BB12Q65R 10PK UC BAL TUB14-8 |
| 00199150034239 - NA | 2025-08-04 CUSTOM PACK 12Q76R VAVD PK |
| 00199150034345 - NA | 2025-08-04 CUSTOM PACK BB11R40R8 TRANS PORT |
| 00199150034352 - NA | 2025-08-04 CUSTOM PACK BB9P03R5 14/38 AV |
| 00199150034369 - NA | 2025-08-04 CUSTOM PACK BB9Q43R4 38/12 AV |
| 20199150034394 - NA | 2025-08-04 CUSTOM PACK BB12N77R1 4PK 3/8 STRAIGHT |