Mediseb Ltd. was established in
late 2000 as a spin-off of SeBo Tecnologies Ltd. to promote
innovative ideas for products in the medical devices field.
Mediseb formally began business operations in 2009 after several
years of performing clinical studies and trials based on the
company's core technology.
Mediseb's experienced management team has brought together a
highly qualified and motivated staff with extensive experience in
medical engineering and development, including outstanding medical
practitioners and scientists.
All Mediseb's projects and products are under continual
medical supervision and evaluation, to ensure that products are
developed in line with medical needs and standards.
Our commitment to quality
Mediseb's goal is to provide high quality products and services
for its clients. The Mediseb quality management
system complies with the requirements defined in DIN EN ISO 13485,
ISO 9001, Annex II of the Medical Device Council Directive
93/42/EEC and the FDA QS Regulation. All employees and managers
at Mediseb are fully committed to complying with these
requirements.