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 2019-07-12 for JACKSON ANG 4MM CUP FCPS 28CM 505100 manufactured by Teleflex Medical.
Report Number | 3011137372-2019-00234 |
MDR Report Key | 8786292 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-07-12 |
Date of Report | 2019-06-19 |
Date of Event | 2019-06-17 |
Date Mfgr Received | 2019-08-01 |
Date Added to Maude | 2019-07-12 |
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 | JASMINE BROWN |
Manufacturer Street | 3015 CARRINGTON MILL BLVD |
Manufacturer City | MORRISVILLE NC 27560 |
Manufacturer Country | US |
Manufacturer Postal | 27560 |
Manufacturer Phone | 9193614124 |
Manufacturer G1 | TELEFLEX MEDICAL |
Manufacturer Street | 3015 CARRINGTON MILL BLVD |
Manufacturer City | MORRISVILLE NC 27560 |
Manufacturer Country | US |
Manufacturer Postal Code | 27560 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | JACKSON ANG 4MM CUP FCPS 28CM |
Generic Name | JACKSON STR 4MM CUP FCPS 28CM |
Product Code | GEN |
Date Received | 2019-07-12 |
Returned To Mfg | 2019-07-17 |
Catalog Number | 505100 |
Lot Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL |
Manufacturer Address | RESEARCH TRIANGLE PARK NC |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-07-12 |