Brand Name | COAGUCHEK XS 2X24 |
Type of Device | TEST, TIME, PROTHROMBIN |
Manufacturer (Section D) |
ROCHE DIAGNOSTICS OPERATIONS, INC. |
|
|
MDR Report Key | 8090724 |
MDR Text Key | 128097819 |
Report Number | MW5081506 |
Device Sequence Number | 1 |
Product Code |
GJS
|
UDI-Device Identifier | 65702012810 |
UDI-Public | 65702-0128-10 |
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Voluntary
|
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
5 Devices were Involved in the Event: |
1
2
3
4
5
|
1 Patient was Involved in the Event |
|
Date FDA Received | 11/19/2018 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
No
|
Device Operator |
No Information
|
Device Lot Number | 30497311 |
Is the Reporter a Health Professional? |
Yes
|
Was Device Evaluated by Manufacturer? |
No Information
|
Type of Device Usage |
N
|
Patient Sequence Number | 1 |
|
|