Dear Users,

HMT Medizintechnik GmbH (HMT) extends our deepest gratitude for your dedication and invaluable contributions to patient care. Your expertise ensures the highest standards of treatment, particularly in cardiopulmonary bypass procedures for cardiac surgery.
As a longstanding manufacturer of cardiopulmonary bypass devices in Europe, we are committed to maintaining the highest safety and performance standards. Under the European Medical Device Regulation (EU) 2017/745 (MDR), we must systematically and proactively monitor our products in the market to ensure their continued safety and effectiveness.
To meet these requirements, we have developed a Post-Market Clinical Follow-up survey for clinical users. This survey is crucial for our technical documentation, involving the collection and evaluation of data on our devices' performance and safety in clinical settings. Your active participation is vital in this regard.
Thank you for your support and collaboration. Together, we can ensure our cardiopulmonary bypass devices adhere to state-of-the-art safety and performance standards, benefiting the patients we all serve.
HMT Medizintechnik GmbH
Frauenstraße 30, 82216 Maisach
Germany
Feel free to reach out to us in case of questions at:
Email: vertrieb@hmt-ffb.de
Phone: +49 (0) 8141 4003-51

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* 1. User

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* 2. Position/Role in Organisation

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* 3. Clinic

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* 4. HMT Contact/Distributor (if known)

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* 5. Variant/Product numbers (if known)

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* 6. In your clinical practise, which of the following medical devices from HMT do you use regularly:

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