Brand Name | MONOCRYL (POLIGLECAPRONE 25) SUTURE |
Type of Device | SUTURE, ABSORBABLE, SYNTHETIC |
Manufacturer (Section D) |
ETHICON INC. |
p.o. box 151, route 22 west |
somerville NJ 08876 015 |
|
Manufacturer (Section G) |
ETHICON INC. - JUAREZ |
avenida de las torres 7125, co |
l salvacar |
ciudad juarez 3260 4 |
MX
32604
|
|
Manufacturer Contact |
guillermo
villa
|
route 22 west po box 151 |
somerville, NJ 08876
|
9082180707
|
|
MDR Report Key | 3781395 |
MDR Text Key | 4435292 |
Report Number | 2210968-2014-05455 |
Device Sequence Number | 1 |
Product Code |
GAN
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K964072 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Health Professional,User Facility |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
04/10/2014 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 04/30/2014 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Expiration Date | 07/31/2016 |
Device Catalogue Number | Y495G |
Device Lot Number | DKZ481 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Date Manufacturer Received | 04/10/2014 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 09/01/2011 |
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) |
Required Intervention;
|