Brand Name | LEVEL 1 FAST FLOW TRAUMA FLUID WARMER, 230 V CONTINENTAL EUROPE |
Type of Device | WARMER, BLOOD, NON-ELECTROMAGNETIC RADIATION |
Manufacturer (Section D) |
SMITHS MEDICAL ASD, INC. |
3350 granada ave n, suite 100 |
oakdale MN 55128 |
|
Manufacturer Contact |
reed
covert
|
6000 nathan lane north |
minneapolis, MN 55442
|
2247062300
|
|
MDR Report Key | 18581158 |
MDR Text Key | 333823088 |
Report Number | 2183161-2024-00104 |
Device Sequence Number | 1 |
Product Code |
BSB
|
Combination Product (y/n) | N |
Reporter Country Code | KS |
PMA/PMN Number | BK020043 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Distributor |
Reporter Occupation |
Non-Healthcare Professional
|
Type of Report
| Initial |
Report Date |
01/25/2024 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 01/25/2024 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Other
|
Device Catalogue Number | 8002937 |
Date Manufacturer Received | 01/02/2024 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 03/05/2019 |
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Patient Sequence Number | 1 |
|
|