Brand Name | ATTUNE PS FEM TRIAL SZ 7 RT |
Type of Device | ATTUNE INSTRUMENTS : FEMORAL TRIALS |
Manufacturer (Section D) |
DEPUY IRELAND - 9616671 |
loughbeg ringaskiddy co. |
cork |
EI |
|
Manufacturer (Section G) |
DEPUY IRELAND - 9616671 |
loughbeg, ringaskiddy co |
|
cork |
EI
|
|
Manufacturer Contact |
kara
ditty-bovard
|
700 orthopaedic dr. |
warsaw, IN 46581-0988
|
6107428552
|
|
MDR Report Key | 12127175 |
MDR Text Key | 260228257 |
Report Number | 1818910-2021-14472 |
Device Sequence Number | 1 |
Product Code |
HWT
|
UDI-Device Identifier | 10603295133995 |
UDI-Public | 10603295133995 |
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,health |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
05/27/2021 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 07/07/2021 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | 2545-00-727 |
Device Catalogue Number | 254500727 |
Device Lot Number | MVMBYX860 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 06/09/2021 |
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 07/01/2021 |
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 03/22/2016 |
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |