INTELLIS Adverse Event — Malfunction (MDR 3004209178-2020-07754)
INTELLIS Adverse Event — Malfunction (MDR 3004209178-2020-07754) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INTELLIS; Generic name: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO..
| Device | INTELLIS |
|---|---|
| Generic name | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 3004209178-2020-07754 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER |
| Narrative | CONCOMITANT MEDICAL PRODUCTS: PRODUCT ID: 977C290, SERIAL#: (B)(4), IMPLANTED: (B)(6) 2018, PRODUCT TYPE: LEAD, PRODUCT ID: 977C290, SERIAL#: (B)(4), IMPLANTED: (B)(6) 2007, EXPLANTED: (B)(6) 2018, PRODUCT TYPE: LEAD. OTHER RELEVANT DEVICE(S) ARE: PRODUCT ID: 977C290, SERIAL/LOT #: (B)(4), UBD: 24-JAN-2022, UDI#: (B)(4); PRODUCT ID: 977C290, SERIAL/LOT #:(B)(4) , UBD: 24-JAN-2022. IF INFORMATION I |
| Source | openFDA MAUDE (device adverse events) |
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