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The reprocessing unit for medical devices (AEMP) is responsible for the reprocessing of medical devices - primarily for the operating theatre (main customer), but also for various departments and external and internal medical practices.
AEMP has been certified in accordance with ISO EN 13485:2016 since November 2013. Compliance with the standard is successfully verified annually in internal and external surveillance audits and every three years as part of re-certifications. The quality policy ensures that all processes, products and services meet the required standards and are consistently orientated towards the needs of customers.
A modern infrastructure, computerised documentation and highly qualified employees underline the commitment to the highest quality and the continuous improvement of product, process and service quality. In 2025, the AEMP's certificate was once again successfully confirmed.
Centralised sterile processing certificate (AEMP)
Size
2.9 MiB
Management and organisation of the AEMP
Petra Wyss
Head of AEMP, service centre operating theatres and intensive care unit
Spital Zollikerberg
Dienstleistungszentrum Operationssäle und Intensivstation
Trichtenhauserstrasse 20
8125 Zollikerberg
ISO certification
We have an ISO-certified quality management system that guarantees the highest standards in the reprocessing and sterilisation of medical devices, including flexible endoscopes.