MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-02-06 for COOLIEF COOLED RADIOFREQUENCY PROBE KIT CRK-17-50-4 104407500 manufactured by Avanos Medical Inc..
Report Number | 8030647-2020-00008 |
MDR Report Key | 9677902 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-02-06 |
Date of Report | 2020-04-01 |
Date of Event | 2020-01-16 |
Date Mfgr Received | 2020-03-23 |
Device Manufacturer Date | 2019-07-04 |
Date Added to Maude | 2020-02-06 |
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 |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | COOLIEF COOLED RADIOFREQUENCY PROBE KIT |
Generic Name | COOLED RF PROBES AND CANNULAS |
Product Code | GXI |
Date Received | 2020-02-06 |
Model Number | CRK-17-50-4 |
Catalog Number | 104407500 |
Lot Number | M19185D208 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
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 | 2020-02-06 |