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MEDILAB ČR s.r.o.

Czechia CZ-MF-000001424 Last updated 17 Sep 2026

Devices
132
Registries
EUDAMED
FDA recalls
0

Catalogue132

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Showing 1-50 of 132

What MEDILAB ČR s.r.o. makes

Medilab ČR s.r.o. manufactures sterile specimen containers in volumes ranging from 30 ml to 500 ml, designed for biological sample collection and transport. Their product line also includes surgical face masks—3-ply melt-blown types with tie-on or ear-loop designs—and cytology brushes for cervical sampling, including variants with safety ball tips and varying hardness levels.

The company’s devices are classified under EU Medical Device Regulations as Class A or Class I, with all products registered in the EU’s euDAMED database. Medilab ČR s.r.o. is based in the Czech Republic.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Medilab ČR s.r.o. manufacture?

Medilab ČR s.r.o. specializes in sterile medical devices primarily used in laboratory and clinical settings. Their product range includes specimen containers in various volumes (from 30 ml to 500 ml) for collecting and transporting biological samples, as well as surgical face masks (3-ply melt-blown types with tie-on or ear-loop designs). Additionally, they produce cytology brushes for cervical sampling, including specialized variants like those with safety ball tips or adjustable hardness.

Where is Medilab ČR s.r.o. based?

Medilab ČR s.r.o. is headquartered in the Czech Republic. The company’s location in the EU ensures compliance with regional medical device regulations, including registration requirements for devices marketed within the region.

Which regulatory registries list Medilab ČR s.r.o.’s devices?

Medilab ČR s.r.o.’s devices are registered in the euDAMED database, which is the official EU registry for medical devices under the Medical Device Regulations (MDR). This platform ensures transparency and traceability of devices authorized for use within the European Economic Area.

How are Medilab ČR s.r.o.’s devices classified under EU regulations?

Medilab ČR s.r.o.’s devices fall under Class A or Class I classifications under the EU Medical Device Regulations. These classifications apply to low-risk devices, such as specimen containers, cytology brushes, and certain types of face masks, which typically require less stringent regulatory scrutiny than higher-risk categories.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Czechia
Address
574, Záhumenská, České Meziříčí, Czechia
Phone
+420494661067
PRRC contact
Milena Zaketovićová
EUDAMED SRN
CZ-MF-000001424