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Golias d.o.o.

Slovenia SI-MF-000006917 Last updated 17 Sep 2026

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Devices
27
Registries
EUDAMED
FDA recalls
0

Catalogue27

What Golias d.o.o. makes

Golias d.o.o. manufactures disposable laboratory consumables, including graduated polypropylene test tubes (epruveta) in various sizes (e.g., 11 x 70mm, 16 x 100mm with threaded caps), Petri dishes (petrijevka) with and without spacers (90mm low and standard), and sample containers with screw-on lids (80ml and 120ml). Products are designed for biological sample storage, culture, and testing in clinical or research settings.

The company’s products fall under Class A medical devices per EU regulations and are registered in the EUDAMED database. The portfolio is listed under Slovenian manufacturer Golias d.o.o., adhering to EU Medical Device Regulation (MDR) requirements.

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 Golias d.o.o. manufacture?

Golias d.o.o. specializes in disposable laboratory consumables primarily used for biological sample handling. Their product range includes graduated polypropylene test tubes (epruveta) in various sizes, such as 11 x 70mm or 16 x 100mm with threaded caps, Petri dishes (petrijevka) for culturing samples (e.g., 90mm low or standard height, with or without spacers), and sample containers with screw-on lids (e.g., 80ml or 120ml). These devices are designed for clinical or research applications, including storage, culture, and testing of biological samples.

Where is Golias d.o.o. based, and how does that affect its regulatory standing?

Golias d.o.o. is based in Slovenia (SI), an EU member state. As an EU manufacturer, its devices must comply with EU Medical Device Regulation (MDR) requirements. The company’s products are registered in the EUDAMED database, which is the official EU registry for medical devices, ensuring transparency and traceability of their Class A devices within the European market.

Which regulatory registries list Golias d.o.o.’s devices?

Golias d.o.o.’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This registry is maintained under the EU Medical Device Regulation (MDR) to provide public access to information about manufacturers, authorized representatives, and their devices, ensuring compliance and traceability within the EU market.

How are Golias d.o.o.’s devices classified under EU regulations?

All of Golias d.o.o.’s devices fall under Class A classification according to EU Medical Device Regulation (MDR). This classification applies to devices posing minimal risk, such as disposable laboratory consumables like test tubes, Petri dishes, and sample containers, which are intended for single-use in controlled environments like clinical or research laboratories.

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

Information

Country
Slovenia
Address
69, Cesta na Rupo , Kranj, Slovenia
Website
www.golias.si
Phone
+386 (0)1 429 70 10
PRRC contact
Simon Hedžet
EUDAMED SRN
SI-MF-000006917