Brand Name | EXALT MODEL D SINGLE-USE DUODENOSCOPE |
Type of Device | DUODENOSCOPE AND ACCESSORIES, FLEXIBLE/RIGID |
Manufacturer (Section D) |
BOSTON SCIENTIFIC CORPORATION |
300 boston scientific way |
marlborough MA 01752 |
|
Manufacturer (Section G) |
BOSTON SCIENTIFIC CORPORATION |
2546 calle primera |
|
alajuela |
CS
|
|
Manufacturer Contact |
carole
morley
|
300 boston scientific way |
marlborough, MA 01752
|
5086834015
|
|
MDR Report Key | 15271485 |
MDR Text Key | 302682779 |
Report Number | 3005099803-2022-04766 |
Device Sequence Number | 1 |
Product Code |
FDT
|
UDI-Device Identifier | 08714729995746 |
UDI-Public | 08714729995746 |
Combination Product (y/n) | N |
Reporter Country Code | IT |
PMA/PMN Number | K193202 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Other,Foreign,Health Professional,Company Representative |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
08/22/2022 |
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 | 08/06/2023 |
Device Model Number | M0054242CE0 |
Device Catalogue Number | 4242CE |
Device Lot Number | 0027794661 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
08/01/2022
|
Initial Date FDA Received | 08/22/2022 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 08/06/2021 |
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 |