MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-27 for METAFIX 579.0004 NOT APPLICABLE manufactured by Corin Medical.
Report Number | 9614209-2020-00031 |
MDR Report Key | 9887618 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-03-27 |
Date of Report | 2020-03-27 |
Date of Event | 2020-03-03 |
Date Mfgr Received | 2020-03-03 |
Device Manufacturer Date | 2018-01-03 |
Date Added to Maude | 2020-03-27 |
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 | MR FRANCK DIDIER |
Manufacturer Street | THE CORINIUM CENTRE CIRENCESTER |
Manufacturer City | GLOUCESTERSHIRE, GL7 1YJ |
Manufacturer Country | UK |
Manufacturer Postal | GL7 1YJ |
Manufacturer G1 | CORIN MEDICAL |
Manufacturer Street | THE CORINIUM CENTRE CIRENCESTER |
Manufacturer City | GLOUCESTERSHIRE, GL7 1YJ |
Manufacturer Country | UK |
Manufacturer Postal Code | GL7 1YJ |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | METAFIX |
Generic Name | HIP STEM |
Product Code | LZO |
Date Received | 2020-03-27 |
Model Number | 579.0004 |
Catalog Number | NOT APPLICABLE |
Lot Number | 372203 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CORIN MEDICAL |
Manufacturer Address | THE CORINIUM CENTRE CIRENCESTER GLOUCESTERSHIRE, GL7 1YJ UK GL7 1YJ |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2020-03-27 |