Brand Name | CAPSURE FIXATION SYSTEM |
Type of Device | STAPLE, IMPLANTABLE |
Manufacturer (Section D) |
DAVOL INC., SUB. C.R. BARD, INC. |
100 crossings blvd. |
warwick RI 02886 |
|
Manufacturer (Section G) |
BARD SHANNON LIMITED -3005636544 |
san geronimo industrial park |
lot #1, road #3, km 79.7 |
humacao PR 00791 |
|
Manufacturer Contact |
anna
smith
|
100 crossings blvd. |
warwick, RI 02886
|
4018258449
|
|
MDR Report Key | 8949415 |
MDR Text Key | 156105595 |
Report Number | 1213643-2019-08096 |
Device Sequence Number | 1 |
Product Code |
GDW
|
UDI-Device Identifier | 00801741094996 |
UDI-Public | (01)00801741094996 |
Combination Product (y/n) | N |
Reporter Country Code | SF |
PMA/PMN Number | K142808 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
foreign,user facility |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
08/30/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 08/30/2019 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 07/28/2019 |
Device Catalogue Number | 0113230 |
Device Lot Number | HUBV0478 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 08/12/2019 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 08/29/2017 |
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 |
|
|