Brand Name | ACCEL® |
Type of Device | BOTTLE, COLLECTION, VACUUM |
Manufacturer (Section D) |
B. BRAUN MELSUNGEN AG |
deli külhatar u. 2 - 4 |
gyöngyös, 3200 |
HU 3200 |
|
Manufacturer (Section G) |
B. BRAUN MELSUNGEN AG |
deli külhatar u. 2 - 4 |
|
gyöngyös, 3200 |
HU
3200
|
|
Manufacturer Contact |
jonathan
severino
|
901 marcon blvd. |
allentown, PA 18109
|
4847197287
|
|
MDR Report Key | 16875407 |
MDR Text Key | 314636995 |
Report Number | 9610825-2023-00197 |
Device Sequence Number | 1 |
Product Code |
KDQ
|
UDI-Device Identifier | 04046964613371 |
UDI-Public | (01)04046964613371 |
Combination Product (y/n) | N |
Reporter Country Code | US |
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 |
06/30/2023 |
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 Model Number | 622275 |
Device Catalogue Number | 622275 |
Device Lot Number | 22M11F0000 |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
04/18/2023
|
Initial Date FDA Received | 05/05/2023 |
Supplement Dates Manufacturer Received | 04/18/2023
|
Supplement Dates FDA Received | 06/30/2023
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 11/11/2022 |
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 |
|
|