Brand Name | SAFEDRAW¿ |
Type of Device | SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE |
Manufacturer (Section D) |
MERIT MEDICAL SINGAPORE PTE LTD. |
198 yishun ave 7 |
singapore, 76892 6 |
SN 768926 |
|
Manufacturer (Section G) |
MERIT MEDICAL SINGAPORE PTE LTD. |
198 yishun ave 7 |
|
singapore, 76892 6 |
SN
768926
|
|
Manufacturer Contact |
bryson
heaton
|
1600 merit parkway |
south jordan, UT 84095
|
|
MDR Report Key | 14048243 |
MDR Text Key | 288875922 |
Report Number | 8020616-2022-00019 |
Device Sequence Number | 1 |
Product Code |
DXN
|
UDI-Device Identifier | 00884450359839 |
UDI-Public | 884450359839 |
Combination Product (y/n) | N |
Reporter Country Code | SW |
PMA/PMN Number | N/A |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,User Facility,Company Representative |
Reporter Occupation |
Other
|
Type of Report
| Initial,Followup |
Report Date |
03/28/2022 |
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 Catalogue Number | 688410/B |
Device Lot Number | C2229852 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
03/28/2022 |
Initial Date FDA Received | 04/07/2022 |
Supplement Dates Manufacturer Received | 04/26/2022
|
Supplement Dates FDA Received | 05/11/2022
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
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 |
|
|