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 2020-03-03 for PINNACLE UTILITY CASE 2220-00-210 222000210 manufactured by Depuy Orthopaedics Inc Us.
Report Number | 1818910-2020-06721 |
MDR Report Key | 9781640 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-03 |
Date of Report | 2020-02-18 |
Date Mfgr Received | 2020-03-09 |
Device Manufacturer Date | 2014-04-11 |
Date Added to Maude | 2020-03-03 |
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 | 700 ORTHOPAEDIC DRIVE |
Manufacturer City | WARSAW IN 465810988 |
Manufacturer Country | US |
Manufacturer Postal | 465810988 |
Manufacturer Phone | 6107428552 |
Manufacturer G1 | DEPUY ORTHOPAEDICS INC US |
Manufacturer Street | 700 ORTHOPAEDIC DRIVE |
Manufacturer City | WARSAW IN 465810988 |
Manufacturer Country | US |
Manufacturer Postal Code | 465810988 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PINNACLE UTILITY CASE |
Generic Name | PROJECT NEPTUNE : INSTRUMENT CASES |
Product Code | FSM |
Date Received | 2020-03-03 |
Returned To Mfg | 2020-03-03 |
Model Number | 2220-00-210 |
Catalog Number | 222000210 |
Lot Number | PV0064220 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY ORTHOPAEDICS INC US |
Manufacturer Address | 700 ORTHOPAEDIC DRIVE WARSAW IN 465810988 US 465810988 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-03 |