Brand Name | BRAVO |
Type of Device | ELECTRODE, PH, STOMACH |
Manufacturer (Section D) |
GIVEN IMAGING LTD., YOQNEAM |
yetsira 13 street |
yoqneam 20692 |
IS 20692 |
|
Manufacturer (Section G) |
GIVEN IMAGING LTD., YOQNEAM |
yetsira 13 street |
|
yoqneam 20692 |
IS
20692
|
|
Manufacturer Contact |
justin
ellis
|
8200 coral sea st ne |
mounds view, MN 55112
|
7635265677
|
|
MDR Report Key | 16754571 |
Report Number | 9710107-2023-00083 |
Device Sequence Number | 1 |
Product Code |
FFT
|
UDI-Device Identifier | 07290101369707 |
UDI-Public | 07290101369707 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K102543 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Health Professional |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
04/17/2023 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 08/28/2024 |
Device Model Number | FGS-0635 |
Device Catalogue Number | FGS-0635 |
Device Lot Number | 59344F |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
03/31/2023 |
Initial Date FDA Received | 04/17/2023 |
Date Device Manufactured | 02/28/2023 |
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
|
|