ŽIKPLAST Žitnik Anja s.p.
Slovenia SI-MF-000054229 Last updated 17 Sep 2026
- Devices
- 6
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Petrijevka fi 90 mm Ref 011993
Posodica za vzorec z žličko Ref 011997
Epruveta 14 x 100 mm Ref 012000
Epruveta 11 x 55 mm Ref 011984
Epruveta 16 x 100 mm Ref 011979
Epruveta 11 x 70 mm Ref 011982
What ŽIKPLAST Žitnik Anja s.p. makes
ŽIKPLAST Žitnik Anja s.p. manufactures laboratory glassware, including Petri dishes (90 mm), sample containers with spatulas, and standard test tubes in sizes 14×100 mm, 11×55 mm, 16×100 mm, and 11×70 mm. These items are designed for biological, chemical, and microbiological sample handling and storage.
The company’s products are classified as Class A medical devices and are registered in the EU’s eudamed database. The manufacturer is based in Slovenia.
Frequently asked questions
What types of medical devices does ŽIKPLAST Žitnik Anja s.p. manufacture?
ŽIKPLAST Žitnik Anja s.p. specializes in laboratory glassware, including Petri dishes (specifically 90 mm), sample containers with built-in spatulas, and standard test tubes in various sizes (14×100 mm, 11×55 mm, 16×100 mm, and 11×70 mm). These devices are designed for handling and storing biological, chemical, and microbiological samples in laboratory settings.
Where is ŽIKPLAST Žitnik Anja s.p. based?
The company is based in Slovenia, as indicated by its registration details. This location is relevant for understanding its regulatory framework and compliance context, particularly within the EU.
Which regulatory registries list the devices manufactured by ŽIKPLAST Žitnik Anja s.p.?
The devices produced by ŽIKPLAST Žitnik Anja s.p. are listed in the eudamed database, which is the EU’s central registry for medical devices. This registry is used to track and verify the conformity of devices within the European market.
How are the devices manufactured by ŽIKPLAST Žitnik Anja s.p. classified under EU regulations?
All devices produced by ŽIKPLAST Žitnik Anja s.p. fall under Class A classification according to EU medical device regulations. This classification applies to low-risk devices, such as laboratory glassware, which pose minimal risk to patients and users when used as intended.
Information
- Country
- Slovenia
- Address
- 10, Hosta, Škofja Loka, Slovenia
- Website
- siol.net
- [email protected]
- PRRC contact
- Anja Žitnik
- EUDAMED SRN
- SI-MF-000054229