MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2019-07-17 for TL, SHORT BOLT, WIRE FIXATION, UNIVERSAL 54-1151 manufactured by Orthofix Srl.
Report Number | 9680825-2019-00047 |
MDR Report Key | 8798313 |
Report Source | DISTRIBUTOR,FOREIGN |
Date Received | 2019-07-17 |
Date of Report | 2019-07-17 |
Date of Event | 2019-05-23 |
Date Mfgr Received | 2019-06-21 |
Date Added to Maude | 2019-07-17 |
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. ROBERTO DONADELLO |
Manufacturer Street | VIA DELLE NAZIONI, 9 |
Manufacturer City | BUSSOLENGO, VERONA, ITALY 37012 |
Manufacturer Country | IT |
Manufacturer Postal | 37012 |
Manufacturer G1 | ORTHOFIX SRL |
Manufacturer Street | VIA DELLE NAZIONI, 9 |
Manufacturer City | BUSSOLENGO, VERONA, 37012 |
Manufacturer Country | IT |
Manufacturer Postal Code | 37012 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TL, SHORT BOLT, WIRE FIXATION, UNIVERSAL |
Generic Name | TL, SHORT BOLT, WIRE FIXATION, UNIVERSAL |
Product Code | LXT |
Date Received | 2019-07-17 |
Returned To Mfg | 2019-06-21 |
Model Number | 54-1151 |
Catalog Number | 54-1151 |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ORTHOFIX SRL |
Manufacturer Address | VIA DELLE NAZIONI, 9 BUSSOLENGO, VERONA, 37012 IT 37012 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-07-17 |