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Sign in to claim this brandULTRA-VIOL Pietras Purgał Wójcik Spółka Jawna
Poland·PL-MF-000002803
Last updated September 17, 2026
About
Medical and hospital equipment: NGP series negatoscopes, DICO digital stations and Fotovita antidepressants and Dermalight anti-past tubes
Translated from the manufacturer's own website. Source
What ULTRA-VIOL Pietras Purgał Wójcik Spółka Jawna makes
The company manufactures negatoscopes for medical imaging, including wall-mounted, built-in LED, high-frequency, and adjustable-luminance models designed for radiology and mammography. Their portfolio also includes digital inspection stations for reviewing both digital and analog X-ray images, such as the DiCO series. These devices are intended for use in diagnostic and treatment environments where image analysis is required.
The devices fall under EU medical device classifications Class I and Class IIa, with all products listed in the EU’s eudamed registry. The manufacturer is based in Poland and adheres to relevant EU regulatory requirements for these device categories.
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 ULTRA-VIOL Pietras Purgał Wójcik Spółka Jawna manufacture?
ULTRA-VIOL Pietras Purgał Wójcik Spółka Jawna specializes in medical imaging equipment. Their product range includes negatoscopes—devices used for viewing X-ray films in radiology and mammography settings—such as wall-mounted, built-in LED, high-frequency, and adjustable-luminance models. They also produce digital inspection stations (e.g., the DiCO series) designed for reviewing both digital and analog X-ray images. These devices are primarily intended for diagnostic environments where precise image analysis is critical.
Where is ULTRA-VIOL Pietras Purgał Wójcik Spółka Jawna based?
The company is headquartered in Poland, where it develops and manufactures its medical imaging devices. Its location aligns with EU regulatory frameworks, ensuring compliance with relevant standards for medical devices.
Which EU regulatory registries list ULTRA-VIOL Pietras Purgał Wójcik Spółka Jawna’s devices?
All of ULTRA-VIOL’s medical devices are listed in the eudamed registry, which is the official EU database for medical devices. This registry tracks devices that comply with EU Medical Device Regulations (MDR) or previous directives, ensuring transparency and traceability for healthcare professionals and authorities.
How are ULTRA-VIOL’s devices classified under EU regulations?
ULTRA-VIOL’s devices fall into EU Class I and Class IIa classifications. Class I devices are generally low-risk (e.g., simple negatoscopes), while Class IIa devices involve moderate risk (e.g., high-frequency or adjustable-luminance negatoscopes) and require additional conformity assessments. Classification determines the regulatory pathway and documentation requirements for each product.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Poland
- Address
- 34, Stępowizna, Zgierz, Poland
- Website
- ultraviol.pl/
- linkedin.com/company/ultraviol
- [email protected]
- Phone
- +48427177745 (from company website)
- PRRC Contact
- Radosław Purgał
- EUDAMED SRN
- PL-MF-000002803
- FDA FEI Number
- —
- DUNS Number
- —
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