Brand Name | BD SPINAL NEEDLE,QUINCKE |
Type of Device | NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER) |
Manufacturer (Section D) |
BECTON, DICKINSON AND COMPANY |
1 becton dr |
franklin lakes NJ 07417 |
|
MDR Report Key | 7112155 |
MDR Text Key | 94658237 |
Report Number | 7112155 |
Device Sequence Number | 1 |
Product Code |
BSP
|
UDI-Device Identifier | 00382904051815 |
UDI-Public | (01)00382904051815 |
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
User Facility
|
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
12/06/2017 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Physician
|
Device Expiration Date | 05/31/2022 |
Device Model Number | 405181 |
Device Catalogue Number | 405181 |
Device Lot Number | 7125998 |
Other Device ID Number | 22G X 3.50IN |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
No
|
Was the Report Sent to FDA? |
Yes
|
Date Report Sent to FDA | 12/06/2017 |
Event Location |
Outpatient Diagnostic Facility
|
Date Report to Manufacturer | 12/06/2017 |
Initial Date Manufacturer Received |
Not provided
|
Initial Date FDA Received | 12/13/2017 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
N
|
Patient Sequence Number | 1 |
|
|