Dermatology in Malta falls under the general medical duty of the Health Care Professions Act (Chapter 464). Practices performing biopsies, excisions, or cryotherapy with reusable instruments fall under EU Medical Devices Regulation expectations.
Dermatologists in Malta who perform surgical procedures — skin biopsies, excisions, cryotherapy with reusable instruments — operate under the general medical duty of the Health Care Professions Act (Chapter 464). Regulation (EU) 2017/745 (Medical Devices Regulation) applies directly to reusable medical devices. The Standards for Dental Clinics (March 2024) is not a dermatology-specific document, but its sterilisation framework — Class B steriliser, validation, cycle checks, load verification — applies as best practice to any clinic processing reusable invasive instruments. HCSD inspection of medical premises follows the Standards' general principles. Documented sterilisation traceability is a core professional obligation under Medical Council of Malta expectations.
Health Care Professions Act (Chapter 464 of the Laws of Malta) · Public Health Act (Chapter 465) · Regulation (EU) 2017/745 (MDR) · EN 13060 · EN ISO 17665-1
Regulatory guides to help you understand your obligations.
Track reusable surgical instrument sterilization
Import your autoclave cycle after each procedure day. Sign the record and maintain a tamper-proof history.
QR-coded labels for instrument traceability
Print traceability labels for each sterilized instrument pack. Link them to the specific autoclave cycle.
Complements your single-use workflow
Most dermatology instruments are single-use — but the ones that aren't need traceable sterilization. SecuSteri handles the reusable portion.
These instruments come pre-loaded when you create your account. You can add, edit, or remove instruments at any time.
Melag, W&H, Castellini, and Anthos reports are imported automatically via AutoReport or manual upload. Other brands? Upload the report or enter cycle data manually — we add automatic support progressively.
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