MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-10-08 for PILLCAM FGS-0517 manufactured by Given Imaging Ltd., Yoqneam.
Report Number | 9710107-2019-00446 |
MDR Report Key | 9166106 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-10-08 |
Date of Report | 2019-10-08 |
Date of Event | 2019-09-10 |
Date Mfgr Received | 2019-09-16 |
Device Manufacturer Date | 2019-07-10 |
Date Added to Maude | 2019-10-08 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | AMY BEEMAN |
Manufacturer Street | 161 CHESHIRE LANE, SUITE 100 |
Manufacturer City | PLYMOUTH MN 55441 |
Manufacturer Country | US |
Manufacturer Postal | 55441 |
Manufacturer Phone | 7632104064 |
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 | PILLCAM |
Generic Name | COLON CAPSULE IMAGING SYSTEM |
Product Code | PGD |
Date Received | 2019-10-08 |
Model Number | FGS-0517 |
Catalog Number | FGS-0517 |
Lot Number | 46735C |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
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 | 1. Hospitalization; 2. Required No Informationntervention | 2019-10-08 |