| Brand Name | SOFTCLIX ® LANCET DEVICE |
| Common Device Name | LANCET DEVICE |
| Manufacturer (Section D) |
| ROCHE DIABETES CARE, INC. |
| 9115 hague road |
| indianapolis IN 46250 -045 |
|
| Manufacturer (Section G) |
| Balda Medical GmbH |
| bergkirchener str. 228 |
| na |
| bad oeyhausen NA 32549 |
|
GM
32549
|
|
| Manufacturer Contact |
|
natalie
catton
|
| 9115 hague road |
| na |
| indianapolis, IN 46250--045
|
|
| MDR Report Key | 50065348 |
| Report Number | 3011393376-2026-00461 |
| Device Sequence Number | 16042532 |
| Product Code |
QRL
|
| UDI-Device Identifier | 04015630082209 |
| UDI-Public | 04015630082209 |
| Combination Product (Y/N) | N |
| Initial Reporter State | NA |
| Initial Reporter Country | US |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Serviced by Third Party (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign |
| Type of Report
| Initial,Followup |
| Report Date (Section B) |
10/02/2026 |
| 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 |
Lay User/Patient
|
| Device Catalogue Number | 05181186001 |
| Device Lot Number | BBK080 |
| Was Device Available for Evaluation? |
No
|
| Is the Reporter a Health Professional? |
No
|
| Initial Date Received by Manufacturer | 07/04/2026 |
| Supplement Date Received by Manufacturer | 09/29/2026
|
| Initial Report FDA Received Date | 07/29/2026 |
| Supplement Report FDA Received Date | 10/02/2026
|
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Date Device Manufactured | 10/30/2024 |
| Is the Device Labeled for Single Use? (Y/N) |
No
|
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 Age | 75 YR |
| Patient Sex | Female |
|
|