Brand Name | ADDEASE® |
Type of Device | SET, I.V. FLUID TRANSFER |
Manufacturer (Section D) |
B. BRAUN MEDICAL INC. |
901 marcon blvd. |
allentown PA 18109 |
|
Manufacturer Contact |
jonathan
severino
|
901 marcon blvd. |
allentown, PA 18109
|
4847197287
|
|
MDR Report Key | 18685024 |
MDR Text Key | 335188358 |
Report Number | 2523676-2024-00131 |
Device Sequence Number | 1 |
Product Code |
LHI
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K090905 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Health Professional,User Facility,Company Representative |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial,Followup |
Report Date |
03/12/2024 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Catalogue Number | BC2000 |
Device Lot Number | 0061880055 |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
01/29/2024
|
Initial Date FDA Received | 02/12/2024 |
Supplement Dates Manufacturer Received | 01/29/2024
|
Supplement Dates FDA Received | 03/12/2024
|
Was Device Evaluated by Manufacturer? |
No
|
Date Device Manufactured | 04/03/2023 |
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 |
|
|