Brand Name | UCENTUM |
Type of Device | SCREW, POLYAXIAL, 7.5MM, LENGTH 50MM |
Manufacturer (Section D) |
ULRICH GMBH & CO. KG |
buchbrunnenweg 12 |
ulm, 89081 |
GM 89081 |
|
Manufacturer (Section G) |
ULRICH GMBH & CO. KG |
buchbrunnenweg 12 |
na |
ulm, 89081 |
GM
89081
|
|
Manufacturer Contact |
christoph
ulrich
|
buchbrunnenweg 12 |
na |
ulm, baden-württemberg 89081
|
GM
89081
|
|
MDR Report Key | 8745579 |
MDR Text Key | 149553152 |
Report Number | 9612420-2019-00040 |
Device Sequence Number | 1 |
Product Code |
NKB
|
UDI-Device Identifier | 04052536161195 |
UDI-Public | 4052536161195 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K123717 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative |
Reporter Occupation |
Non-Healthcare Professional
|
Type of Report
| Initial |
Report Date |
01/12/2017,06/27/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 06/28/2019 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | CS 3802-075-050 |
Device Catalogue Number | CS 3802-075-050 |
Device Lot Number | U012976 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 01/16/2017 |
Was the Report Sent to FDA? |
No
|
Distributor Facility Aware Date | 01/12/2017 |
Date Report to Manufacturer | 01/12/2017 |
Date Manufacturer Received | 01/16/2017 |
Was Device Evaluated by Manufacturer? |
Yes
|
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 |
Patient Outcome(s) |
Hospitalization;
|
|
|