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 2019-11-22 for C-STEM PMMA END CAP 961226000 manufactured by Depuy International Ltd - 8010379.
Report Number | 1818910-2019-117602 |
MDR Report Key | 9363241 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-11-22 |
Date of Report | 2019-10-28 |
Date of Event | 2019-11-21 |
Date Mfgr Received | 2019-11-22 |
Device Manufacturer Date | 2009-10-01 |
Date Added to Maude | 2019-11-22 |
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 | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | KARA DITTY-BOVARD |
Manufacturer Street | 700 ORTHOPAEDIC DR. |
Manufacturer City | WARSAW IN 465810988 |
Manufacturer Country | US |
Manufacturer Postal | 465810988 |
Manufacturer Phone | 6107428552 |
Manufacturer G1 | DEPUY INT'L LTD. 8010379 |
Manufacturer Street | ST ANTHONYS ROAD |
Manufacturer City | LEEDS LS118 DT |
Manufacturer Country | UK |
Manufacturer Postal Code | LS11 8 DT |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | C-STEM PMMA END CAP |
Generic Name | HIP MISCELLANEOUS : CEMENT CENTRALIZER/PLUG |
Product Code | JDK |
Date Received | 2019-11-22 |
Catalog Number | 961226000 |
Lot Number | 2967886 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY INTERNATIONAL LTD - 8010379 |
Manufacturer Address | ST. ANTHONY'S ROAD LEEDS LS118DT UK LS11 8DT |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-11-22 |