Brand Name | MEDOS VENTRICULAR CATHETER |
Type of Device | SHUNT, CENTRAL NERVOUS SYSTEM & COMPS |
Manufacturer (Section D) |
CODMAN & SHURTLEFF, INC. / MEDOS S.A. |
rue girardet 29 |
ch-2400 le locle |
SZ |
|
Manufacturer Contact |
james
kenney
|
325 paramount drive |
raynham, MA 02767
|
5088282726
|
|
MDR Report Key | 5928592 |
MDR Text Key | 53927030 |
Report Number | 1226348-2016-10630 |
Device Sequence Number | 1 |
Product Code |
JXG
|
Combination Product (y/n) | N |
Reporter Country Code | CH |
PMA/PMN Number | K053350 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,foreig |
Reporter Occupation |
Medical Equipment Company Technician/Representative
|
Type of Report
| Initial |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Expiration Date | 06/30/2018 |
Device Catalogue Number | 82-3041 |
Device Lot Number | CPGDC4 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
08/19/2016 |
Initial Date FDA Received | 09/06/2016 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 10/01/2013 |
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 |
Treatment | 82-3045; 82-3112 |
Patient Outcome(s) |
Required Intervention;
|