Dermatologists practice in healthcare facilities — the same reprocessing obligations under D.Lgs 81/2008 and the ISPESL guidelines apply in full to dermatology and aesthetic medicine.
Dermatology and aesthetic medicine are healthcare activities regulated by the general framework of D.Lgs 81/2008 Title X. There is no dermatology-specific sterilization regulation — the 2010 ISPESL Linee Guida and UNI/TR 11408:2011, which apply to all healthcare facilities, are the references. Because these practices may involve reusable instruments (curettes, biopsy forceps, minor surgical instruments), the reprocessing and traceability obligation is that of a healthcare facility. The Legge Gelli-Bianco (Law 24/2017) applies in full to dermatologists as to any healthcare professional: documented sterilization is evidence in any professional liability proceeding.
D.Lgs 81/2008, Title X · ISPESL Linee Guida May 2010 · UNI/TR 11408:2011 · UNI EN 13060 · Law 24/2017 (Gelli-Bianco)
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.
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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