MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-11-07 for BRAVO FGS-0636 manufactured by Given Imaging Ltd., Yoqneam.
Report Number | 9710107-2019-00534 |
MDR Report Key | 9293362 |
Report Source | USER FACILITY |
Date Received | 2019-11-07 |
Date of Report | 2019-11-07 |
Date Mfgr Received | 2019-10-23 |
Device Manufacturer Date | 2019-07-18 |
Date Added to Maude | 2019-11-07 |
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 | LISA HERNANDEZ |
Manufacturer Street | 60 MIDDLETOWN AVE |
Manufacturer City | NORTH HAVEN CT 06473 |
Manufacturer Country | US |
Manufacturer Postal | 06473 |
Manufacturer Phone | 2034925563 |
Manufacturer G1 | GIVEN IMAGING LTD., YOQNEAM |
Manufacturer Street | YETSIRA 13 STREET |
Manufacturer City | YOQNEAM 20692 |
Manufacturer Postal Code | 20692 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BRAVO |
Generic Name | SYSTEM, IMAGING, GASTROINTESTINAL, WIRELESS, CAPSULE |
Product Code | NEZ |
Date Received | 2019-11-07 |
Returned To Mfg | 2019-10-29 |
Model Number | FGS-0636 |
Catalog Number | FGS-0636 |
Lot Number | 46590F |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | GIVEN IMAGING LTD., YOQNEAM |
Manufacturer Address | YETSIRA 13 STREET YOQNEAM 20692 20692 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-07 |