Brand Name | BLOOD GROUPING REAGENT ANTI-A |
Type of Device | SERACLONE ANTI-A |
Manufacturer (Section D) |
BIO-RAD MEDICAL DIAGNOSTICS GMBH |
industriestrasse 1 |
dreieich, 63303 |
GM 63303 |
|
Manufacturer (Section G) |
BIO-RAD MEDICAL DIAGNOSTICS GMBH |
industriestrasse 1 |
|
dreieich, 63303 |
GM
63303
|
|
Manufacturer Contact |
martina
benkert
|
industriestrasse 1 |
dreieich, hessen 63303
|
GM
63303
|
|
MDR Report Key | 8882768 |
MDR Text Key | 219482407 |
Report Number | 9610824-2019-00046 |
Device Sequence Number | 1 |
Product Code |
KSZ
|
UDI-Device Identifier | 07611969950065 |
UDI-Public | (01)07611969950065(17)200220(10)8808030-03 |
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
health professional,user faci |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
08/12/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 08/12/2019 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 02/20/2020 |
Device Catalogue Number | 801325100 |
Device Lot Number | 8808030-03 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 07/30/2019 |
Date Manufacturer Received | 07/15/2019 |
Was Device Evaluated by Manufacturer? |
Yes
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |