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Sign in to claim this brandMar-Four Siekierska, Titienko S.C.
Poland·PL-MF-000036041
Last updated May 23, 2026
What Mar-Four Siekierska, Titienko S.C. makes
The company produces laboratory glassware and histological embedding media, including microscope slides (cover and base slides in various colors and sizes, such as blue, white, orange, pink, and yellow), paraffin wax for tissue processing, and formalin-filled surgical containers. Their product range also includes hematatoxylin, a staining reagent used in histology for preparing tissue samples.
These devices are classified under Class A in the EU Medical Device Regulation (MDR), and the manufacturer lists them in the euDAMED registry. The company operates from Poland.
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 Mar-Four Siekierska, Titienko S.C. manufacture?
Mar-Four Siekierska, Titienko S.C. specializes in laboratory glassware and histological embedding media. Their products include microscope slides (base and cover slides in various colors and sizes), paraffin wax for tissue processing, formalin-filled surgical containers, and hematatoxylin—a staining reagent used in histology to prepare tissue samples for examination.
Where is Mar-Four Siekierska, Titienko S.C. based?
The company is based in Poland, as indicated by its country of origin. This location is relevant for regulatory compliance and reporting purposes under EU medical device regulations.
Which regulatory registries list the devices manufactured by Mar-Four Siekierska, Titienko S.C.?
The manufacturer lists its devices in the euDAMED registry, which is the European database for medical devices. This registry is used to track and verify medical devices authorized under EU regulations, ensuring transparency and traceability.
How are the devices produced by Mar-Four Siekierska, Titienko S.C. classified under EU regulations?
All devices manufactured by Mar-Four Siekierska, Titienko S.C. fall under Class A classification in the EU Medical Device Regulation (MDR). This classification applies to low-risk devices, such as laboratory glassware and certain histological reagents, which pose minimal risk to patients and users.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Poland
- Address
- 5/7, Srebrzyńska, Konstantynów Łódzki, Poland
- Website
- www.marfour.com.pl
- —
- —
- [email protected]
- Phone
- +48 42 650 88 21
- PRRC Contact
- Justyna Olczak
- EUDAMED SRN
- PL-MF-000036041
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (32)
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