| Primary Device ID | 00613994300546 |
| NIH Device Record Key | 3786bd1b-12f3-4635-95bf-c57d3f0441bc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PISCES-QUAD PLUS |
| Version Model Number | 3888-33 |
| Company DUNS | 796986144 |
| Company Name | MEDTRONIC, 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 | 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 | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Length | 33 Centimeter |
| Length | 33 Centimeter |
| Length | 33 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994300546 [Primary] |
| LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
| 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 | 2014-09-23 |
| 00613994300560 | LEAD 3888-56 PISCES QD 12MM SP US MKT |
| 00613994300553 | LEAD 3888-45 PISCES QD 12MM SP US MKT |
| 00613994300546 | LEAD 3888-33 PISCES QD 12MM SP US MKT |