Medical Device

… You develop the ideas, we can help you navigate through challenges of preclinical research

The main goal of biological evaluation of medical devices is to ensure that materials and products that come into contact with the human body are biocompatible – that is, that they do not cause undesirable biological reactions.

Regulation: Regulation (EU) 2017/745 on medical devices (MDR)

Tests for systemic toxicity

Single & Repeated dose studies including TK evaluation, rodent & non-rodent species

Test for irritation and skin sensitization

Single & Repeated dose studies, rodent species

Test for local effects after implantation

Implantation tests evaluate the body’s reaction to materials placed inside tissue.
These tests help ensure that medical devices are safe for human use and meet regulatory standards.

Single & Repeated dose/Implantation studies, rodent & non-rodent species

Address

MediTox s.r.o.,
Pod Zámkem 279,
281 25 Konárovice, Czech Republic

E-mail

business@meditox.eu project.manager@meditox.eu

company ID

25926713

vat number

CZ25926713

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