| Brand Name | SINGLE USE BIOPSY VALVE (Sterile) |
| Common Device Name | SINGLE USE BIOPSY VALVE |
| Manufacturer (Section D) |
| OLYMPUS MEDICAL SYSTEMS CORP. Hinode Plant |
| 34-3 hirai, hinode-machi |
| nishitama-gun, tokyo 190-0 182 |
| JA 190-0182 |
|
| Manufacturer (Section G) |
| OLYMPUS MEDICAL SYSTEMS CORP. Hinode Plant |
| 34-3 hirai, hinode-machi |
|
| nishitama-gun, tokyo 190-0 182 |
|
JA
190-0182
|
|
| Manufacturer Contact |
|
todd
brill
|
| 800 west park drive |
| westborough, MA 01581
|
|
+1(508)207-7661
|
|
| MDR Report Key | 50221417 |
| Report Number | 3003637092-2026-00156 |
| Device Sequence Number | 18721061 |
| Product Code |
EOQ
|
| UDI-Device Identifier | 14953170152433 |
| UDI-Public | 14953170152433 |
| Combination Product (Y/N) | N |
| Initial Reporter Country | JA |
| PMA/510(K) Number | K061313 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Foreign,User Facility |
| Initial Reporter Occupation |
Non-Healthcare 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 | MAJ-210 |
| Device Lot Number | H5X05 |
| Was Device Available for Evaluation? |
Yes
|
| Is the Reporter a Health Professional? |
No
|
| Initial Date Received by Manufacturer | 07/23/2026 |
| Initial Report FDA Received Date | 08/12/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
No
|
| 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 |
Reuse
|
| Patient Sequence Number | 1 |
| Patient Sex | Unknown |
|
|