Brand Name | WHIN ONE INFUSION |
Type of Device | 22GA X 3/4"HUBER NEEDLE WITH Y SET |
Baseline Device 510(K) Number | |
Baseline Device PMA Number | |
Manufacturer (Section D) |
B. BRAUN MEDICAL, INC. |
824 twelfth ave. |
bethlehem PA 18018 |
|
Device Event Key | 158342 |
MDR Report Key | 162629 |
Event Key | 152848 |
Report Number | MW1013499 |
Device Sequence Number | 1 |
Product Code | FMI |
Report Source |
Voluntary
|
Report Date |
04/06/1998 |
1 Device Was Involved in the Event | |
1 Patient Was Involved in the Event | |
Date FDA Received | 04/06/1998 |
Is This An Adverse Event Report? |
No
|
Is This A Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Catalogue Number | HW2276YHRF |
OTHER Device ID Number | STOCK #1610 |
Was Device Available For Evaluation? |
Yes
|
Is the Device an Implant? |
No
|
Is this an Explanted Device? |
No Answer Provided
|
Patient TREATMENT DATA |
Date Received: 04/06/1998 Patient Sequence Number: 1 |
# | Treatment | Treatment Date |
1,NOT APPLICABLE, |
|
|
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