Brand Name | EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE |
Type of Device | GASTROINTESTINAL VIDEOSCOPE |
Manufacturer (Section D) |
AIZU OLYMPUS CO., LTD. |
3-1-1 niiderakita |
aizuwakamatsu-shi, fukushima 965-8 520 |
JA 965-8520 |
|
Manufacturer (Section G) |
AIZU OLYMPUS CO., LTD. |
3-1-1 niiderakita |
|
aizuwakamatsu-shi, fukushima |
|
Manufacturer Contact |
todd
brill
|
800 west park drive |
westborough, MA 01581
|
5082077661
|
|
MDR Report Key | 16033007 |
MDR Text Key | 305976715 |
Report Number | 9610595-2022-05873 |
Device Sequence Number | 1 |
Product Code |
FDS
|
Combination Product (y/n) | N |
Reporter Country Code | SP |
PMA/PMN Number | K112680 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Other,Foreign,Study,Literature,Health Professional,User Facility,Company Representative |
Reporter Occupation |
Physician
|
Type of Report
| Initial,Followup |
Report Date |
02/09/2023 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Model Number | GIF-1TH190 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Was the Report Sent to FDA? |
No
|
Initial Date Manufacturer Received |
11/21/2022
|
Initial Date FDA Received | 12/22/2022 |
Supplement Dates Manufacturer Received | 01/27/2023
|
Supplement Dates FDA Received | 02/09/2023
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Patient Sequence Number | 1 |
Treatment | NON-OLYMPUS, ELECTROSURGICAL GENERATOR; NON-OLYMPUS, HOT-AXIOS; NON-OLYMPUS, JAGWIRE; NON-OLYMPUS, WALLFLEX DUODENAL; OLYMPUS 4.5F 3-LUMEN BALLOON-V; OLYMPUS 7F NASAL-BILIARY DRAINAGE TUBE-V; OLYMPUS, GF-UCT180 |
Patient Outcome(s) |
Required Intervention;
|
|
|