
Clinic Risk Assessments
COSHH - UVC and Ozone Disinfection
COSHH RISK ASSESSMENT FORM
Ultraviolet-C and Ozone Sterilisation Device
HAUS OF ÄSTHETIK
Location: 4 Portland Square, Water Street, Bakewell, Derbyshire, DE45 1HA, United Kingdom
Date of Assessment: 1st April 2025 Review Date: 1st April 2026 Assessed By: Managing Director
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Product Name: 200W Dual-Action UV-C & Ozone Room Steriliser
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Manufacturer:
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Supplier:
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COSHH Safety Data Sheet Available? ☑ Yes ☐ No
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Wavelengths:
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UV-C: 254 nm (germicidal wavelength for DNA/RNA disruption)
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Ozone-generating: 185 nm (ozone production spectrum)
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Technology: Ultraviolet germicidal irradiation (UVGI) and ozone-based air purification
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Auto Safety Mechanism: Infrared motion detector auto shut-off if human presence is detected during operation
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Location of Use: Clinical treatment rooms, waiting area, reception, and toilet facilities.
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How is it used?
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Operated nightly or in response to known or suspected contamination risk.
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Used to sterilise enclosed, unoccupied rooms via UV-C and ozone.
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Who is Exposed?
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Practitioners, cleaning staff, and patients if not properly controlled.
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Frequency of Use: Daily (60-minute cycle at close of business) or as needed.
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Hazard Classification:
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☑ Irritant (ozone inhalation)
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☑ Mutagenic (UV-C exposure)
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☑ Harmful if inhaled (ozone in high concentrations)
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Potential Hazards:
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Eye or skin injury from direct UV-C exposure
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Respiratory irritation from ozone accumulation
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Material degradation (rubber, silicone, plastics) from ozone
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Electrical fault/fire hazard if misused
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Symptoms of Exposure:
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UV-C: Erythema (skin redness), photokeratitis ("welder's flash"), skin burns
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Ozone: Coughing, throat irritation, dizziness, metallic or chlorine-like smell
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A. Storage & Handling
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☑ Keep device unplugged when not in use
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☑ Store in a clean, dry, low-dust environment
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☑ Do not tamper with auto shut-off sensors
B. Use Protocol
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☑ Device must only be operated in unoccupied rooms
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☑ Duration per treatment: 60 minutes for room size 5m x 4m
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☑ Use during close of business or after known contamination event
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☑ Room must be vented post-treatment:
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5–10 minutes (low wind)
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30 minutes (good ventilation or sunny weather)
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☑ If ozone smell remains (metallic/bleach-like), vent for another 10–20 minutes
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☑ Avoid use near rubber or exposed silicone devices
C. Personal Protective Equipment (PPE)
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☑ No PPE required during correct usage (device must be operated in unoccupied rooms only)
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☑ If venting manually: wear nitrile gloves and a Type IIR mask if residual ozone scent is strong
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UV-C Overexposure:
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Leave area immediately
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Flush exposed skin or eyes with cold water
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Seek medical attention if symptoms persist
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Ozone Inhalation:
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Move to fresh air
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Monitor breathing and seek medical advice if irritation or symptoms persist
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☑ Weekly visual inspection of lamp and sensor functionality
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☑ Annual servicing by the manufacturer or approved technician
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☑ Log every use of the device:
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Date/time
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Duration
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Operator name
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Post-treatment ventilation completed
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☑ Malfunctions must be reported and logged
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Overall Risk Level (After Controls Applied): ☑ Low
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Are current controls sufficient? ☑ Yes ☐ No
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Additional Control Measures Required? ☐ Yes ☑ No
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☑ All staff must be trained in:
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Proper operation of the UV/Ozone steriliser
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COSHH awareness regarding ozone
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Emergency response procedures
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☑ Annual refresher training required
Assessor Name: Owen Dickinson
Role: Managing Director
Signature: ___________________
Date: 1st April 2025