MKBClass II
Device, Germicidal, Ultraviolet
General Hospital · 21 CFR 880.6500
MDR events18All time
Recalls0All time
Registered firms1Currently listed
510(k) clearances0All time
Recent MDR events
18 adverse event reports on file
- Unnamed deviceFeb 3, 2025No answer providedCOR25000058-000
- Unnamed deviceApr 23, 2024OtherCOR24000069-000
- Unnamed deviceJan 18, 2024OtherCOR24000014-000
- Unnamed deviceJan 18, 2024OtherCOR24000015-000
- Unnamed deviceDec 22, 2023OtherCOR23000253-000
- Unnamed deviceDec 22, 2023OtherCOR23000254-000
- Unnamed deviceDec 22, 2023OtherCOR23000255-000
- Unnamed deviceDec 22, 2023OtherCOR23000256-000
- Unnamed deviceDec 22, 2023OtherCOR23000257-000
- Unnamed deviceDec 22, 2023OtherCOR23000258-000
Event type breakdown
Other12
No answer provided3
Malfunction2
Injury1
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
1 firms currently registered for this product code
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.