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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.

Medical staff in surgical clothing sorting instruments in the hospital.

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

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Management and organisation of the AEMP

Portrait photo

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.

  • For patient referrals to the IPS:

    Tel +41 44 397 20 68 (Mon - Fri, 7.00 a.m. - 5.00 p.m.)

    Tel +41 44 397 21 42 (Mon - Fri, 5.00 pm - 7.00 am and on weekends and public holidays)

    Dienstleistungszentrum Operationssäle und Intensivstation
    Trichtenhauserstrasse 20
    8125 Zollikerberg