Brand Name | BD PERISAFE¿ EPIDURAL MINI-KIT |
Type of Device | ANESTHESIA CONDUCTION KIT |
Manufacturer (Section D) |
BD CARIBE LTD. |
road 31 |
k.m. 24.3 |
juncos |
|
Manufacturer (Section G) |
BD CARIBE LTD. |
road 31 |
k.m. 24.3 |
juncos |
|
Manufacturer Contact |
brett
wilko
|
9450 south state street |
sandy, UT 84070
|
8015652845
|
|
MDR Report Key | 7433310 |
MDR Text Key | 105771878 |
Report Number | 2618282-2018-00011 |
Device Sequence Number | 1 |
Product Code |
CAZ
|
UDI-Device Identifier | 30382904002733 |
UDI-Public | 30382904002733 |
Combination Product (y/n) | N |
Reporter Country Code | IN |
PMA/PMN Number | K953790 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
foreign,health professional,o |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
04/02/2018 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 04/16/2018 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Other
|
Device Expiration Date | 05/31/2021 |
Device Catalogue Number | 400273 |
Device Lot Number | 6123765 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 03/22/2018 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 06/21/2016 |
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) |
Other;
|