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"KRIOMEDPOL" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

Poland·PL-MF-000033911

Last updated September 17, 2026

About

Leader of cryotherapy and cryosurgery equipment industry. Our products are valued by doctors and physiotherapists because they know that they can rely on their effectiveness and reliability.

Translated from the manufacturer's own website. Source

What "KRIOMEDPOL" SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ makes

Kriomedpol produces reusable hot and cold therapy packs designed for therapeutic applications, including models like the Kriopol R50 Bryza II, Kriopol R30 Bryza II, and Kriopol K20 Bora. These devices are intended for controlled temperature-based treatments in clinical and physiotherapy settings.

The company’s products fall under EU Class IIa medical devices and are registered in the EU’s eudamed database. The manufacturer is based in 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 Kriomedpol manufacture?

Kriomedpol specializes in reusable hot and cold therapy packs, which are primarily used for therapeutic applications. These devices are designed to deliver controlled temperature treatments, such as cryotherapy or heat therapy, in clinical and physiotherapy environments. Examples include models like the Kriopol R50 Bryza II, Kriopol R30 Bryza II, and Kriopol K20 Bora.

Where is Kriomedpol based, and what region does it serve?

Kriomedpol is headquartered in Poland. While the company’s exact market reach isn’t specified, its products are intended for use in clinical and physiotherapy settings, which suggests a focus on European and potentially global markets where Class IIa medical devices are regulated.

Which regulatory registries list Kriomedpol’s devices?

Kriomedpol’s devices are listed in the eudamed database, which is the EU’s central registry for medical devices. This registration is required for devices placed on the European market, ensuring traceability and compliance with EU medical device regulations.

How are Kriomedpol’s devices classified under EU regulations?

Kriomedpol’s hot and cold therapy packs fall under EU Class IIa classification. This classification is assigned based on the device’s intended purpose and associated risks—Class IIa devices pose a moderate risk and require additional measures like design controls and risk management to ensure safety and performance.

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

Information

Country
Poland
Address
272, Warszawska, Stare Babice, Poland
Phone
—
PRRC Contact
Cezary Fijałkowski
EUDAMED SRN
PL-MF-000033911
FDA FEI Number
—
DUNS Number
—

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Kriopol R50 Bryza II 5905610730710
EUDAMED
Class IIaActive
Kriopol R30 Bryza II 5905610730512
EUDAMED
Class IIaActive
Kriopol K20 Bora 5905610731106
EUDAMED
Class IIaActive

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