Brand Name | QUICKSET RATCHET SCDR HDL |
Type of Device | HIP INSTRUMENTS : HANDLES |
Manufacturer (Section D) |
. DEPUY ORTHOPAEDIC INC, 1818910 |
700 orthopaedic drive |
warsaw IN 46582 0988 |
|
Manufacturer (Section G) |
DEPUY ORTHOPAEDIC INC, 1818910 |
700 orthopaedic drive |
|
warsaw IN 46582 |
|
Manufacturer Contact |
chad
gibson
|
700 orthopaedic drive |
warsaw, IN 46582-0988
|
5743725905
|
|
MDR Report Key | 7518118 |
MDR Text Key | 108490993 |
Report Number | 1818910-2018-59737 |
Device Sequence Number | 1 |
Product Code |
HXX
|
UDI-Device Identifier | 10603295109020 |
UDI-Public | 10603295109020 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | NI |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,health |
Reporter Occupation |
Health Professional
|
Type of Report
| Initial,Followup |
Report Date |
04/20/2018 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 05/16/2018 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Catalogue Number | 227402000 |
Device Lot Number | BS0802 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 04/30/2018 |
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 07/03/2018 |
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 08/15/2002 |
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 |