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 2019-06-05 for INJECTION NEEDLE CATHETER 60817 991092774 manufactured by Avanos Medical Inc..
Report Number | 8030647-2019-00052 |
MDR Report Key | 8670947 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-06-05 |
Date of Report | 2019-07-18 |
Date of Event | 2019-04-29 |
Date Mfgr Received | 2019-07-01 |
Device Manufacturer Date | 2018-01-17 |
Date Added to Maude | 2019-06-05 |
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 | OTHER HEALTH CARE PROFESSIONAL |
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 | INJECTION NEEDLE CATHETER |
Generic Name | DH ENDOSCOPY INJECTION NEEDLE CATHETERS |
Product Code | KDH |
Date Received | 2019-06-05 |
Returned To Mfg | 2019-05-22 |
Model Number | 60817 |
Catalog Number | 991092774 |
Lot Number | M18011E112 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
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 | 2019-06-05 |