| Brand Name | VITROS Chemistry Products PHYT Slides |
| Common Device Name | In-Vitro Diagnostics |
| Manufacturer (Section D) |
| Ortho-Clinical Diagnostics, Inc. |
| 100 indigo creek drive |
| rochester NY 14626 |
|
| Manufacturer (Section G) |
| Ortho-Clinical Diagnostics, Inc. |
| 513 technology boulevard |
|
| rochester NY 14626 |
|
| Manufacturer Contact |
|
nancy
hewitson
|
| 100 indigo creek drive |
| rochester, NY 14626
|
|
+1(585)453-4165
|
|
| MDR Report Key | 50858751 |
| Report Number | 1319809-2026-00137 |
| Device Sequence Number | 9554059 |
| Product Code |
DIP
|
| UDI-Device Identifier | 10758750004690 |
| Combination Product (Y/N) | N |
| 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 |
Health Professional |
| Initial Reporter Occupation |
Other Health Care Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
09/22/2026 |
| 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 | 8298671 |
| Device Lot Number | 2631-0202-6053 |
| 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 | 08/27/2026 |
| Initial Report FDA Received Date | 09/22/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
Yes
|
| Date Device Manufactured | 05/20/2026 |
| 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
|
| Patient Sequence Number | 1 |
| Patient Sex | Unknown |
|
|