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Chirana Progress, s.r.o.

Slovakia SK-MF-000016090 Last updated 17 Sep 2026

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Devices
27
Registries
EUDAMED
FDA recalls
0

Catalogue27

About

The production of physiotherapy equipment in Chirana ZQXK000KXZ follows the tradition of production in Chirana Piešťany, which dates back to 1961. Products throughout their history have been valued for their quality and reliability. Also today, Chirany Progress products are associated not only with tradition, but especially with high quality, as demonstrated by ISO 9001:2015 and ISO 13485:2016 production of medical devices.

Translated from the manufacturer's own website. Source

What Chirana Progress, s.r.o. makes

Chirana Progress manufactures physiotherapy devices, including hydrotherapy baths (e.g., Ocean Forte, Hubbard bath, Laguna Plus Bubble), lymphatic drainage systems (e.g., Coral Lymfo, Coral Economy), and bubble bath units (e.g., Cascade Deluxe, Cascade Senior). Additional offerings include underwater massage systems (e.g., Ocean De Luxe, Electra CG) and hydrotherapy accessories like the VOD 56 HT and Lastura.

The company’s products are classified as Class IIa medical devices and are listed in the EU’s eudamed registry. Chirana Progress operates from Slovakia (SK) and adheres to ISO 9001:2015 and ISO 13485:2016 standards for medical equipment manufacturing.

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 Chirana Progress, s.r.o. manufacture?

Chirana Progress, s.r.o. specializes in physiotherapy devices, focusing on hydrotherapy solutions. Their product range includes hydrotherapy baths like the Ocean Forte and Hubbard bath, lymphatic drainage systems such as Coral Lymfo and Coral Economy, underwater massage systems like Ocean De Luxe and Electra CG, and bubble bath units including Cascade Deluxe and Cascade Senior. They also produce accessories like the VOD 56 HT and Lastura, which support hydrotherapy treatments.

Where is Chirana Progress, s.r.o. based, and what regulatory standards do they follow?

Chirana Progress, s.r.o. is based in Slovakia (SK). While the company adheres to ISO 9001:2015 and ISO 13485:2016 standards for quality and medical device manufacturing, these certifications apply to their production processes rather than regulatory approvals for individual devices. Compliance with these standards ensures their manufacturing practices meet international benchmarks for quality and safety.

Are Chirana Progress’s devices listed in any regulatory registries, and if so, which ones?

Yes, Chirana Progress’s devices are listed in the eudamed registry, which is the EU’s central database for medical devices. Listing in eudamed is required for manufacturers to demonstrate compliance with EU Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR) and to provide transparency about their products in the European market.

How are Chirana Progress’s physiotherapy devices classified under EU regulations?

Chirana Progress’s devices are classified as Class IIa medical devices under EU regulations. This classification is determined by factors such as the intended use, risk associated with the device, and its interaction with the body. Class IIa devices pose a moderate risk and require compliance with specific design controls, clinical evaluations, and conformity assessment procedures to ensure safety and performance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Slovakia
Address
17, Vrbovská cesta, Piešťany, Slovakia
Phone
+421337956211
PRRC contact
Andrej Racík
EUDAMED SRN
SK-MF-000016090