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 2019-11-08 for ENDOBON XENOGRAFT GRANULES 2.0ML ROX20 manufactured by Biomet France S.a.r.l..
Report Number | 3006946279-2019-00475 |
MDR Report Key | 9294994 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-11-08 |
Date of Report | 2019-11-08 |
Date of Event | 2017-06-27 |
Date Mfgr Received | 2019-10-11 |
Device Manufacturer Date | 2016-09-19 |
Date Added to Maude | 2019-11-08 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. CHRISTINA ARNT |
Manufacturer Street | 56 E. BELL DR. |
Manufacturer City | WARSAW IN 46582 |
Manufacturer Country | US |
Manufacturer Postal | 46582 |
Manufacturer Phone | 5745273773 |
Manufacturer G1 | BIOMET FRANCE S.A.R.L. |
Manufacturer Street | PLATEAU DE LAUTAGNE BP75 |
Manufacturer City | VALENCE CEDEX 26903 |
Manufacturer Country | FR |
Manufacturer Postal Code | 26903 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ENDOBON XENOGRAFT GRANULES 2.0ML |
Generic Name | BONE GRAFTING MATERIAL, SYNTHETIC |
Product Code | LYC |
Date Received | 2019-11-08 |
Catalog Number | ROX20 |
Lot Number | W0075265 |
Device Expiration Date | 2018-02-28 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOMET FRANCE S.A.R.L. |
Manufacturer Address | PLATEAU DE LAUTAGNE BP75 VALENCE CEDEX 26903 FR 26903 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2019-11-08 |