MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-17 for DLCS08651-01 USED CS20P US N manufactured by Covidien Mfg Plainfield.
| Report Number | 3008361498-2020-00001 |
| MDR Report Key | 9844609 |
| Report Source | USER FACILITY |
| Date Received | 2020-03-17 |
| Date of Report | 2020-03-17 |
| Date of Event | 2020-02-18 |
| Date Mfgr Received | 2020-02-18 |
| Device Manufacturer Date | 2014-03-13 |
| Date Added to Maude | 2020-03-17 |
| 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 |
| Manufacturer Contact | AVI KLUGER |
| Manufacturer Street | 5920 LONGBOW DRIVE |
| Manufacturer City | BOULDER CO 80301 |
| Manufacturer Country | US |
| Manufacturer Postal | 80301 |
| Manufacturer Phone | 3035306582 |
| Manufacturer G1 | COVIDIEN MFG PLAINFIELD |
| Manufacturer Street | 2824 AIRWEST BLVD |
| Manufacturer City | PLAINFIELD IN 46168 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 46168 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DLCS08651-01 USED CS20P US N |
| Product Code | CCK |
| Date Received | 2020-03-17 |
| Model Number | DLCS08651-01 |
| Catalog Number | DLCS08651-01 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN MFG PLAINFIELD |
| Manufacturer Address | 2824 AIRWEST BLVD PLAINFIELD IN 46168 US 46168 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-17 |