MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-10-08 for BIOSTOP G CEM RESTR 12MM 546312000 manufactured by Depuy Cmw - 9610921.
Report Number | 1818910-2019-108307 |
MDR Report Key | 9166364 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-10-08 |
Date of Report | 2019-09-16 |
Date of Event | 2019-09-16 |
Date Mfgr Received | 2019-09-16 |
Device Manufacturer Date | 2016-12-12 |
Date Added to Maude | 2019-10-08 |
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 | 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 CMW - 9610921 |
Manufacturer Street | CORNFORD RD |
Manufacturer City | BLACKPOOL FY4 4QQ |
Manufacturer Country | UK |
Manufacturer Postal Code | FY4 4QQ |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BIOSTOP G CEM RESTR 12MM |
Generic Name | DEPUY CMW RESORBABLE BIOMATERIALS : CEMENT CENTRALIZER/PLUG |
Product Code | JDK |
Date Received | 2019-10-08 |
Catalog Number | 546312000 |
Lot Number | 16E3103005 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DEPUY CMW - 9610921 |
Manufacturer Address | CORNFORD RD BLACKPOOL FY4 4QQ UK FY4 4QQ |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-10-08 |