Brand Name | ALBT2 TINA-QUANT ALBUMIN GEN.2 |
Type of Device | ALBUMIN IMMUNOLOGICAL TEST SYSTEM |
Manufacturer (Section D) |
ROCHE DIAGNOSTICS |
9115 hague road |
indianapolis IN 46250 0457 |
|
Manufacturer (Section G) |
ROCHE DIAGNOSTICS GMBH |
sandhofer strasse 116 |
|
mannheim (baden-wurttemberg) 68305 |
GM
68305
|
|
Manufacturer Contact |
amy
nelson
|
9115 hague road |
indianapolis, IN 46250
|
|
MDR Report Key | 18980530 |
MDR Text Key | 338624004 |
Report Number | 1823260-2024-00915 |
Device Sequence Number | 1 |
Product Code |
DCF
|
UDI-Device Identifier | 04015630920587 |
UDI-Public | 04015630920587 |
Combination Product (y/n) | Y |
Reporter Country Code | SF |
PMA/PMN Number | K101203 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional,User Facility |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial,Followup |
Report Date |
04/19/2024 |
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 | 04469658190 |
Device Lot Number | ASKU |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
03/11/2024
|
Initial Date FDA Received | 03/26/2024 |
Supplement Dates Manufacturer Received | Not provided
|
Supplement Dates FDA Received | 04/19/2024
|
Was Device Evaluated by Manufacturer? |
Yes
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |