| Brand Name | HF-resection electrode, loop, 24 Fr., 0.2 wire, medium, 12° |
| Common Device Name | HF-resection electrode |
| Manufacturer (Section D) |
| Olympus Medical Products Czech, spol. s r.o. |
| telickova 457/29 |
| prerov 75124 |
| EZ 75124 |
|
| Manufacturer (Section G) |
| Olympus Medical Products Czech, spol. s r.o. |
| telickova 457/29 |
|
| prerov 75124 |
|
EZ
75124
|
|
| Manufacturer Contact |
|
todd
brill
|
| 801 west park drive |
| westborough, MA 01581
|
|
+1(508)207-7661
|
|
| MDR Report Key | 50230385 |
| Report Number | 3007960282-2026-00139 |
| Device Sequence Number | 16020635 |
| Product Code |
FAS
|
| UDI-Device Identifier | 14042761051665 |
| UDI-Public | 14042761051665 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | US |
| PMA/510(K) Number | K100275 / K |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign,Health Professional |
| Initial Reporter Occupation |
Other Health Care Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
08/12/2026 |
| 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 Model Number | WA22302D |
| Is the Reporter a Health Professional? |
Yes
|
| Initial Date Received by Manufacturer | 07/23/2026 |
| Initial Report FDA Received Date | 08/13/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| Date Device Manufactured | 05/29/2025 |
| 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 |
Unknown
|
| Patient Sequence Number | 1 |
| Patient Age | 43 YR |
| Patient Sex | Male |
|
|