MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2020-03-30 for LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR 99507-000090 manufactured by Physio-control, Inc. - 3015876.
Report Number | 0003015876-2020-00447 |
MDR Report Key | 9900802 |
Report Source | FOREIGN |
Date Received | 2020-03-30 |
Date of Report | 2020-03-30 |
Date of Event | 2020-03-05 |
Date Mfgr Received | 2020-03-06 |
Device Manufacturer Date | 2016-01-19 |
Date Added to Maude | 2020-03-30 |
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 |
Reporter Occupation | BIOMEDICAL ENGINEER |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. TODD BANDY |
Manufacturer Street | 11811 WILLOWS ROAD NE |
Manufacturer City | REDMOND WA 98052 |
Manufacturer Country | US |
Manufacturer Postal | 98052 |
Manufacturer Phone | 4258674000 |
Manufacturer G1 | PHYSIO-CONTROL, INC. - 3015876 |
Manufacturer Street | 11811 WILLOWS ROAD NE |
Manufacturer City | REDMOND WA 98052 |
Manufacturer Country | US |
Manufacturer Postal Code | 98052 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR |
Generic Name | AUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE) |
Product Code | MKJ |
Date Received | 2020-03-30 |
Returned To Mfg | 2020-03-11 |
Model Number | 20E |
Catalog Number | 99507-000090 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHYSIO-CONTROL, INC. - 3015876 |
Manufacturer Address | 11811 WILLOWS ROAD NE REDMOND WA 98052 US 98052 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-30 |