Golias d.o.o.
Slovenia SI-MF-000006917 Last updated 17 Sep 2026
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- Devices
- 27
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Epruveta 12 x 70mm Ref EP03
Epruveta za določanje sedimentacije Ref EP44
Posodica za vzorec s pokrovom 120ml Ref PO37
Epruveta 16 x 70mm Ref EP05
Epruveta 12 x 75mm Ref EP103
Epruveta 14 x 100mm Ref EP06
Epruveta 16 x 100mm Ref EP04
Petrijevkafi 90mm nizka Ref PE18
Petrijevka fi 90mm L Ref PE01L
Posodica 80ml zaskočni pokrov Ref PO41
Epruveta 16 x 100mm Ref EP108
Epruveta 11 x 70mm Ref EP02
Posodica za vzorec z žličko Ref PO12
Epruveta za določanje sedimentacije Ref EP42
Epruveta 12 x 75mm Ref EP01
Petrijevka fi 90mm K Ref PE01K
Petrijevka fi 90mm z 2 prekati Ref PE19
Petrijevka fi 70mm Ref PE02
Petri dish fi 90mm ster. A Ref PE22A
Posodica za vzorec s pokrovom Ref PO100
Posodica za vzorec z žličko Ref PO102
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.
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.
Information
- Country
- Slovenia
- Address
- 69, Cesta na Rupo , Kranj, Slovenia
- Website
- www.golias.si
- [email protected]
- Phone
- +386 (0)1 429 70 10
- PRRC contact
- Simon Hedžet
- EUDAMED SRN
- SI-MF-000006917