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Sign in to claim this brandALFA VITA, s.r.o.
Czechia·CZ-MF-000051941
Last updated September 17, 2026
About
ALFA VITA, s.r.o., has been active on the Czech health market since 1992 and has been focusing on the production and professional distribution of products to pharmacies, hospitals and medical facilities through medical distributors and business chains.
Translated from the manufacturer's own website. Source
What ALFA VITA, s.r.o. makes
Alfa Vita manufactures reusable manual limb tourniquets and a range of adhesive medical tapes and strips, including fluorescent and colored variants for clinical and sports use. Products include stretch tapes, sensitive adhesive strips, and pre-packaged first aid mixes, designed for medical and patient care applications.
All devices fall under EU Class I regulation and are listed in the EUDAMED registry. The company 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 ALFA VITA, s.r.o. manufacture?
ALFA VITA, s.r.o. specializes in reusable manual limb tourniquets and a variety of adhesive medical tapes and strips. Their product range includes stretch tapes (like FIXAtape STRETCH), sensitive adhesive strips (such as FIXAplast SENSITIVE), and pre-packaged first aid mixes (e.g., FIXAplast FIRST AID FAMILY MIX). These devices are designed for clinical, sports, and patient care applications, with some variants featuring fluorescent or colored designs for visibility or specific use cases.
Where is ALFA VITA, s.r.o. based, and what does this mean for its regulatory compliance?
ALFA VITA, s.r.o. is based in the Czech Republic, which places its devices under EU regulatory oversight. Since all its products fall under EU Class I classification, they must comply with EU Medical Device Regulations (MDR) or EU Medical Device Directives (MDD), depending on the applicable timeline. The company’s devices are listed in the EUDAMED registry, which is the official EU database for medical devices, ensuring transparency and traceability for regulatory authorities.
Which regulatory registries list ALFA VITA’s medical devices?
ALFA VITA’s medical devices are listed in the EUDAMED registry, the official EU database for medical devices. This registry is maintained by the European Commission and is used to track devices under the EU Medical Device Regulations (MDR) or Directives (MDD). Listing in EUDAMED confirms the device’s compliance with EU requirements and provides a public reference for regulatory oversight.
How are ALFA VITA’s devices classified under EU regulations?
All of ALFA VITA’s devices are classified as EU Class I, which is the lowest risk category under EU medical device regulations. This classification applies to products like adhesive tapes, strips, and reusable manual tourniquets, which pose minimal risk to patients when used as intended. Class I devices typically require basic conformity assessment procedures, such as self-certification by the manufacturer, to demonstrate compliance with EU safety and performance standards.
Why do some of ALFA VITA’s adhesive tapes come in fluorescent or colored variants?
The fluorescent and colored variants of ALFA VITA’s adhesive tapes (e.g., FIXAtape STRETCH in green or patterned designs) are likely designed for visibility and practicality in clinical or sports settings. Fluorescent colors improve visibility under low light or in emergency situations, while specific patterns (like bear paw prints) may help distinguish between different product types or applications. These variations cater to user preferences and functional needs without altering the core medical purpose of the tapes.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Czechia
- Address
- 339/2, Starolázeňská, Praha 5, Czechia
- Website
- www.alfavita.cz
- —
- facebook.com/alfavitacz
- [email protected]
- Phone
- +420 604260078
- PRRC Contact
- Miroslav Vlček
- EUDAMED SRN
- CZ-MF-000051941
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (72)
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