MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2020-02-18 for PICCO MONITORING KIT PV8115 manufactured by Pulsion Medical Systems Se.
Report Number | 3003263092-2020-00002 |
MDR Report Key | 9719472 |
Report Source | DISTRIBUTOR,FOREIGN,HEALTH PR |
Date Received | 2020-02-18 |
Date of Report | 2020-03-03 |
Date of Event | 2019-12-19 |
Date Mfgr Received | 2020-03-03 |
Date Added to Maude | 2020-02-18 |
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 | MS. SEVDE GUENGOER |
Manufacturer Street | HANS-RIEDL-STRASSE 17 |
Manufacturer City | FELDKIRCHEN 85622 |
Manufacturer Country | GM |
Manufacturer Postal | 85622 |
Manufacturer Phone | 0894599140 |
Manufacturer G1 | PULSION MEDICAL SYSTEMS SE |
Manufacturer Street | HANS-RIEDL-STRASSE 17 |
Manufacturer City | FELDKIRCHEN 85622 |
Manufacturer Country | GM |
Manufacturer Postal Code | 85622 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PICCO MONITORING KIT |
Generic Name | PROBE, THERMODILUTION |
Product Code | KRB |
Date Received | 2020-02-18 |
Returned To Mfg | 2020-02-26 |
Catalog Number | PV8115 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PULSION MEDICAL SYSTEMS SE |
Manufacturer Address | HANS-RIEDL-STRASSE 17 FELDKIRCHEN 85622 GM 85622 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-18 |