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 TRUMATCH CT CUT GUIDE KIT R 420916 manufactured by Depuy Ireland - 9616671.
Report Number | 1818910-2020-04087 |
MDR Report Key | 9676142 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-02-06 |
Date of Report | 2020-01-21 |
Date of Event | 2020-01-21 |
Date Mfgr Received | 2020-03-04 |
Device Manufacturer Date | 2000-05-25 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. KARA DITTY-BOVARD |
Manufacturer Street | 1210 WARD AVENUE |
Manufacturer City | WEST CHESTER PA 193800988 |
Manufacturer Country | US |
Manufacturer Postal | 193800988 |
Manufacturer Phone | 6107428552 |
Manufacturer G1 | DEPUY RAYNHAM, A DIV. OF DEPUY ORTHO 1219655 |
Manufacturer Street | 325 PARAMOUNT DRIVE |
Manufacturer City | RAYNHAM MA 02767 |
Manufacturer Country | US |
Manufacturer Postal Code | 02767 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TRUMATCH CT CUT GUIDE KIT R |
Generic Name | TRUMATCH INSTRUMENTS : RESECTION BLOCKS/DEVICES |
Product Code | FSM |
Date Received | 2020-02-06 |
Returned To Mfg | 2020-02-26 |
Model Number | 420916 |
Catalog Number | 420916 |
Lot Number | 21380 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY IRELAND - 9616671 |
Manufacturer Address | LOUGHBEG RINGASKIDDY CO. CORK EI |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-06 |