MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-07-03 for SMITHS MEDICAL PORTEX THERMOVENT? HEAT AND MOISTURE EXCHANGER FILTERS 002823P manufactured by .
Report Number | 3012307300-2019-02863 |
MDR Report Key | 8757557 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-07-03 |
Date of Report | 2019-06-27 |
Date of Event | 2019-06-01 |
Date Mfgr Received | 2019-06-03 |
Date Added to Maude | 2019-07-03 |
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 | DAVE HALVERSON |
Manufacturer Street | 6000 NATHAN LANE NORTH |
Manufacturer City | MINNEAPOLIS MN 55442 |
Manufacturer Country | US |
Manufacturer Postal | 55442 |
Manufacturer Phone | 7633833310 |
Manufacturer G1 | SMITHS MEDICAL, ASD INC. |
Manufacturer Street | BOUNDARY ROAD |
Manufacturer City | KENT, |
Manufacturer Country | UK |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SMITHS MEDICAL PORTEX THERMOVENT? HEAT AND MOISTURE EXCHANGER FILTERS |
Generic Name | FILTER, BACTERIAL, BREATHING-CIRCUIT |
Product Code | CAH |
Date Received | 2019-07-03 |
Catalog Number | 002823P |
Lot Number | LT1807 |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Life Threatening; 2. Other; 3. Required No Informationntervention | 2019-07-03 |