
Mahir Çelen
General Manager
Hemera Medikal is an ISO 13485-certified, TITCK-licensed medical device distributor representing 12 brands.
Hemera Medikal was founded in Istanbul in 2006 by two biomedical engineers. Today we are the Turkish distributor of 12 international brands in anaesthesia and intensive care, imaging, laboratory, operating theatre and sterilisation, patient room and consumable groups, serving more than 1,400 hospitals, clinics, medical laboratories and oral and dental health centres.
We stock the devices of the brands we represent in our TITCK-licensed warehouses, register them in UTS, carry out installation and user training, and provide authorised service and calibration after the warranty period. For consumables we prepare scheduled delivery plans that make stock management easier for clinics and laboratories.
Our sales team does not apply pressure; it listens to your need and does not recommend a product that does not meet your hospital's technical specification. Every quotation shows the device price, consumable cost, service and training items separately, so you see the total cost of ownership from the start. Our after-sales commitments are written and attached to the contract.
Our quality policy and materiovigilance procedure are open to everyone on this site. If you have any doubt about a product, simply fill in the reporting form.
Each year we set aside part of our income for device donations to district health centres in need and for biomedical technician training. The internship programme we run with universities gives 20 biomedical engineering students field experience every year.
Every product carries the CE (MDR) mark and is registered in UTS; documents and UDI data are supplied with delivery.
28 certified technicians, six regional service points and on-site maintenance contracts.
Documented hands-on training for physicians, nurses and biomedical staff at every installation.
2-8 °C reagent transport in vehicles with temperature loggers; 48-hour delivery for in-stock items.
Technical specification review, conformity documents and a ready paperwork set for EKAP processes.

General Manager

Quality and Regulatory Manager

Sales Engineer – Imaging and Monitoring

Laboratory Solutions Specialist
Our biomedical engineer will call you within the same working day.