Dermatology in Switzerland falls under the general medical duty of the Medical Professions Act (MedBG, SR 811.11). Practices performing biopsies, excisions, or cryotherapy with reusable instruments fall under MePV Art. 71/72 for reusable medical devices.
Dermatologists in Switzerland who perform invasive procedures — skin biopsies, excisions, cryotherapy with reusable instruments — operate under the Medical Professions Act (MedBG, SR 811.11) and the Medical Devices Ordinance (MePV, SR 812.213) Art. 71 and 72 for any reusable medical devices. Switzerland is NOT within the direct scope of the EU Medical Devices Regulation — MePV is the governing law, harmonized with EU law via SN EN ISO standards under the Schweiz-EU MRA. The GPA 2022 and Class B compliance with SN EN 13060 apply as best practice to any practice processing invasive reusable instruments. Documented traceability is expected by the Kantonsarztamt under MePV Art. 72.
MedBG (SR 811.11) · MePV / ODim (SR 812.213) Art. 71 and 72 · HMG / LPTh (SR 812.21) · GPA 2022 · SN EN 13060 · SN 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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