MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-24 for PANETTI SUCTION INSTRUMENTS 30-1860 manufactured by Spiggle & Theis Medizintechnik Gmbh.
| Report Number | 1926681-2019-05231 |
| MDR Report Key | 8641792 |
| Date Received | 2019-05-24 |
| Date Added to Maude | 2019-05-24 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | PANETTI SUCTION INSTRUMENTS |
| Generic Name | TUBE, EAR SUCTION |
| Product Code | JZF |
| Date Received | 2019-05-24 |
| Model Number | 30-1860 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | SPIGGLE & THEIS MEDIZINTECHNIK GMBH |
| Manufacturer Address | JEDMED; 5416 JEDMED CT ST. LOUIS MO 63129 US 63129 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-05-24 |