Brand Name | BHR |
Type of Device | ACETLR CUP HAP 52MM W/ IMPTR |
Manufacturer (Section D) |
SMITH & NEPHEW ORTHOPAEDICS LTD |
1 kingmaker court |
gallows hill CV34 6WG |
UK CV34 6WG |
|
Manufacturer (Section G) |
SMITH & NEPHEW ORTHOPAEDICS LTD |
aurora house |
spa park |
leamington spa CV31 3HL |
UK
CV31 3HL
|
|
Manufacturer Contact |
terry
mcmahon
|
970 lake carillon drive |
baar |
st. petersburg, FL 33716
|
0628320660
|
|
MDR Report Key | 4368014 |
MDR Text Key | 5260375 |
Report Number | 3005477969-2014-00605 |
Device Sequence Number | 1 |
Product Code |
NXT
|
Combination Product (y/n) | N |
Reporter Country Code | UK |
PMA/PMN Number | P040033 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Company Representative,company representative |
Reporter Occupation |
Medical Equipment Company Technician/Representative
|
Type of Report
| Initial,Followup |
Report Date |
12/30/2014 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 12/30/2014 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Expiration Date | 05/31/2015 |
Device Model Number | 74120152 |
Device Catalogue Number | 74120152 |
Device Lot Number | 10EW27867 005 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 12/10/2014 |
Is the Reporter a Health Professional? |
No
|
Date Manufacturer Received | 12/10/2014 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 05/31/2010 |
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;
Required Intervention;
|