MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-09-27 for SEDLINE KIT 26619 9513 manufactured by Masimo - 52 Discovery.
Report Number | 3011353843-2019-00068 |
MDR Report Key | 9132097 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2019-09-27 |
Date of Report | 2019-08-28 |
Date of Event | 2019-08-28 |
Date Mfgr Received | 2019-10-31 |
Device Manufacturer Date | 2019-05-31 |
Date Added to Maude | 2019-09-27 |
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 | STEFAN LISSMANN |
Manufacturer Street | 52 DISCOVERY |
Manufacturer City | IRVINE CA 926181604 |
Manufacturer Country | US |
Manufacturer Postal | 926181604 |
Manufacturer Phone | 9492977168 |
Manufacturer G1 | MASIMO - MEXICALI |
Manufacturer Street | INDUSTRIAL VALLERA DE MEXICALI CALZADA DEL ORO, NO.2001 |
Manufacturer City | MEXICALI, BAJA CALIFORNIA 21600 |
Manufacturer Country | MX |
Manufacturer Postal Code | 21600 |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SEDLINE KIT |
Generic Name | MONITOR, PHYSIOLOGICAL, PATIENT (WITHOUT ARRHYTHMIA DETECTION OR ALARMS) |
Product Code | MWI |
Date Received | 2019-09-27 |
Returned To Mfg | 2019-10-15 |
Model Number | 26619 |
Catalog Number | 9513 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MASIMO - 52 DISCOVERY |
Manufacturer Address | 52 DISCOVERY IRVINE CA 926181604 US 926181604 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-09-27 |