MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,litera report with the FDA on 2020-02-17 for UNKNOWN COOLED RF PROBES AND CANNULAS manufactured by Avanos Medical Inc..
Report Number | 8030647-2020-00016 |
MDR Report Key | 9717591 |
Report Source | COMPANY REPRESENTATIVE,LITERA |
Date Received | 2020-02-17 |
Date of Report | 2020-02-17 |
Date Mfgr Received | 2020-01-27 |
Date Added to Maude | 2020-02-17 |
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 | MS. LISA CLARK |
Manufacturer Street | 5405 WINDWARD PARKWAY |
Manufacturer City | ALPHARETTA GA 30004 |
Manufacturer Country | US |
Manufacturer Postal | 30004 |
Manufacturer Phone | 4704485444 |
Manufacturer G1 | AVENT S DE RL DE CV |
Manufacturer Street | CARRETERA INTERNACIONAL SALIDA NORTE NO. 1053 |
Manufacturer City | MAGDALENA, CP 84160 |
Manufacturer Country | MX |
Manufacturer Postal Code | 84160 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNKNOWN COOLED RF PROBES AND CANNULAS |
Generic Name | COOLED RF PROBES AND CANNULAS |
Product Code | GXI |
Date Received | 2020-02-17 |
Model Number | UNKNOWN |
Catalog Number | UNKNOWN |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | AVANOS MEDICAL INC. |
Manufacturer Address | 5405 WINDWARD PARKWAY ALPHARETTA GA 30004 US 30004 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-02-17 |