| Brand Name | HARMONYAIR |
| Common Device Name | EQUIPMENT BOOM |
| Manufacturer (Section D) |
| STERIS CORPORATION |
| 2720 gunter park drive east |
| montgomery AL 36109 |
|
| Manufacturer (Section G) |
| STERIS CORPORATION |
| 2720 gunter park drive east |
|
| montgomery AL 36109 |
|
| Manufacturer Contact |
|
daniel
davy
|
| 5960 heisley road |
| mentor, OH 44060
|
|
4402597401
|
|
| MDR Report Key | 25761046 |
| Report Number | 1043572-2026-00063 |
| Device Sequence Number | 21278925 |
| Product Code |
FQO
|
| UDI-Device Identifier | 00724995156718 |
| UDI-Public | (01)00724995156718(11)241217 |
| Combination Product (Y/N) | N |
| Initial Reporter State | CA |
| 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 |
User Facility |
| Initial Reporter Occupation |
Other Health Care Professional
|
| Type of Report
| Initial |
| Report Date (Section B) |
07/09/2026 |
| 1 Device was Involved in the Event |
|
| 1 Patient was Involved in the Event |
|
| Is this an Adverse Event Report? |
Yes
|
| Is this a Product Problem Report? |
No
|
| Operator of Device |
Health Professional
|
| Device Model Number | HARMONYAIR CEILING BOOMS |
| Device Catalogue Number | HMSLM |
| 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 | 06/12/2026 |
| Initial Report FDA Received Date | 07/09/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
Yes
|
| Date Device Manufactured | 12/17/2024 |
| 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 |
Reuse
|
| Patient Sequence Number | 1 |
| Patient Sex | Unknown |