| Brand Name | EASYPUMP |
| Common Device Name | PUMP, INFUSION, ELASTOMERIC |
| Manufacturer (Section D) |
| B. Braun Melsungen AG |
| carl-braun strabe 1 |
| melsungen, hessen 34212 |
| GM 34212 |
|
| Manufacturer (Section G) |
| B. Braun Melsungen AG |
| carl-braun strabe 1 |
|
| melsungen, hessen 34212 |
|
GM
34212
|
|
| Manufacturer Contact |
|
elena
reifenstein
|
| 824 12th ave |
| bethlehem, PA 18018
|
|
+1(833)425-1464
|
|
| MDR Report Key | 50928025 |
| Report Number | 9610825-2026-00523 |
| Device Sequence Number | 16133695 |
| Product Code |
MEB
|
| UDI-Device Identifier | 04046964448638 |
| Combination Product (Y/N) | N |
| Initial Reporter State | UT |
| Initial Reporter Country | US |
| PMA/510(K) Number | K081905 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Health Professional,User Facility |
| Initial Reporter Occupation |
Other Health Care Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
09/29/2026 |
| 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
|
| Operator of Device |
Health Professional
|
| Device Catalogue Number | 4540018-02 |
| Device Lot Number | 24N13GE561 |
| Was Device Available for Evaluation? |
Yes
|
| Is the Reporter a Health Professional? |
Yes
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 09/10/2026 |
| Initial Report FDA Received Date | 09/29/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Date Device Manufactured | 12/13/2024 |
| Is the Device Labeled for Single Use? (Y/N) |
Yes
|
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Usage of Device |
Initial
|
| Patient Sequence Number | 1 |
| Patient Sex | Unknown |
|
|