Brand Name | 16X100 MM 8.5 ML BD VACUTAINER® PLUS PLASTIC SST TUBE |
Type of Device | BLOOD COLLECTION TUBE |
Manufacturer (Section D) |
BECTON, DICKINSON & CO., (BD) |
1575 airport road |
sumter SC 29153 |
|
Manufacturer (Section G) |
BECTON, DICKINSON & CO., (BD) |
1575 airport road |
|
sumter SC 29153 |
|
Manufacturer Contact |
brett
wilko
|
9450 south state street |
sandy, UT 84070
|
8015652845
|
|
MDR Report Key | 7072999 |
MDR Text Key | 93851756 |
Report Number | 1024879-2017-00894 |
Device Sequence Number | 1 |
Product Code |
JKA
|
UDI-Device Identifier | 00382903679881 |
UDI-Public | 00382903679881 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K023075 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
other,user facility |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
11/01/2017 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 11/30/2017 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Other
|
Device Expiration Date | 03/31/2017 |
Device Catalogue Number | 367988 |
Device Lot Number | 6104889 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 09/27/2016 |
Is the Reporter a Health Professional? |
No
|
Date Manufacturer Received | 09/19/2016 |
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 04/13/2016 |
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;
|
|
|