MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-26 for MILAGRO INSCR SMALL SIZE 5X30 231804 manufactured by Depuy Mitek Llc Us.
Report Number | 1221934-2020-00990 |
MDR Report Key | 9883969 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-03-26 |
Date of Report | 2020-03-12 |
Date of Event | 2020-03-10 |
Date Mfgr Received | 2020-04-02 |
Device Manufacturer Date | 2017-10-26 |
Date Added to Maude | 2020-03-26 |
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 | KARA DITTY-BOVARD |
Manufacturer Street | 325 PARAMOUNT DRIVE |
Manufacturer City | RAYNHAM MA 02767 |
Manufacturer Country | US |
Manufacturer Postal | 02767 |
Manufacturer Phone | 6103142063 |
Manufacturer G1 | MEDOS INT MITEK |
Manufacturer Street | CHEMIN BLANC 38 |
Manufacturer City | LE LOCLE 02400 |
Manufacturer Country | SZ |
Manufacturer Postal Code | 02400 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MILAGRO INSCR SMALL SIZE 5X30 |
Generic Name | ORTHOPAEDIC BONE SCREW, BIOABSORBABLE |
Product Code | MAI |
Date Received | 2020-03-26 |
Model Number | 231804 |
Catalog Number | 231804 |
Lot Number | L630312 |
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 MITEK LLC US |
Manufacturer Address | 325 PARAMOUNT DRIVE RAYNHAM MA 02767 US 02767 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-26 |