KrioSystem Sp. z o. o. was established in 1991 r. Its beginnings, however, go back further, to 1974 as the company is carrying on the work of Kriopan, the experimental Department of the Institute of Low Temperatures of the Polish Academy of Sciences. KrioSystem specializes in cryogenic technologies. Using our own designs we manufacture cryogenic equipment applied in medicine, science and industry. With reference to medical equipment our offer includes: cryochambers for performing the whole-body cryotherapy treatments, devices for the local cryotherapy – KRIOSAN and cryosurgery devices – KS-2....

f £ Oirodek Badawczo-Rozwojowy PREDOM-OBR H>J—^ |—1 (K\/WJ~V/1 /\. C Toting & Research Centre PREDOM-OBR \rA n(l IPXQJI M \s ^ \ #2-255 WARSZA WA; POLSKA - POLAND Zapewnienie Jakosci Wyrobu Product Quality Assurance Dyrektywa 93/42/EWG dot. wyrob6w medycznych zmieniona Dyrektywa, 2007/47/WE, Zatacznik VI Directive 93/42/EEC on Medical devices amended by the Directive 2007/47/ EC. Annex VI Jednostka notyfikowana - Osrodek Badawczo-Rozwojowy PREDOM- OBR przeprowadzit audit systemu zapewnienia jakosci wyrobu zgodnie z zatacznikiem VI do Dyrektywy 93/42/EWG (zmienionej Dyrektywa, 2007/47/WE) i stwierdza,...

1. Technical specifications of the rooms The integral part of whole body cryotherapy procedures – especially in regards to locomotor disorders – are physical exercises (kinesiotherapy) and they are crucial to the size of the area required for the effective operation of cryotherapy. Our cryochamber KR-2010 S can treat 20-30 patients for a period of one hour, but not more than 150 patients in one session. After such a serie of procedures, it is required to defrost and regenerate the cryochambers. The operating duration of a chamber is primarily conditioned by the social infrastructure and applicable...

2. Primary parameters of cryochamber The KR-2010 S cryochamber is a prefabricated device, which is installed and started-up in full by the KRIOSYSTEM company. The investor is just responsible for the room preparation according to the previously agreed plan and for the supply of power in the technical room. The installation of the chamber takes place in a completely finished area, apart from the flooring outside the chamber’s area and any possible building works (finishing stage) connected with covering the space between the chamber and the room’s ceiling. The details are agreed upon during the...

number of patients at any one time – between 2 and 4 people, depending on the disability degree; cooling agent – liquid nitrogen; therapeutic temperature range: -110 C to -160 C; automatic control via a touch screen PLC, after input of the operating parameters; constant monitoring of oxygen level in the treatment chamber; audio system between the therapist and the patient;; safety systems – oxygen level in the treatment chamber and the antechamber is constantly monitored. If the level falls below 19%, the chamber is automatically turned off and the screen displays an appropriate message. In addition,...

Nominal operating conditions: Ambient temperature:  Recommended relative humidity:  Power supply:  Voltage and frequency: Working parameters of the cryochamber: Maximum number of patients in the chamber:  Range of operating temperatures in treatment chamber  (programmable): Temperature in pre-chamber:  Treatment duration – programmable range:  Parametry eksploatacyjne: Temperature stabilization in the treatment chamber:  Cryochamber cooling time:  Quantity of respiratory air introduced into the cryochamber:  Oxygen concentration in the cryochamber:  Usage of cooling agent for cooling:...

The investor is solely responsible for the supply of the cooling agent. Liquid nitrogen is currently manufactured and supplied by the following companies: Air Products, Linde, Messer, Air Liquide. The supplier of the cooling agent at the same time supplies the container (based on a lease agreement). The investor is obliged to just prepare the foundation plate for the container – according to the specifications of the container supplier – for the particular container type with an EC Certificate. 4. Cryochamber supply conditions:  Delivery and start-up timeline – 6 weeks from signing of the agreement,...

It is also possible to modify the size of a cryochamber, if the size or character of the room where the cryochamber is to be installed require these kind of changes. KRIOSYSTEM offers help in the preparation of detailed technical specifications related to the location of the KR-2010 S cryochamber in the investor’s building. We can also prepare the designs for the organisational structure, operating methods and the necessary equipment of the health care facility operating within the realms of rehabilitation. The details and the operating conditions are to be agreed upon during the signing of the...

chronic inflammation of the cervical spine painful shoulder syndrome periartheritis (tendinitis), bursitis and muscle inflammation fibromyalgia syndrome (soft tissue rheumatic disease) dislocations and joint sprains due to trauma meniscus injury tearing of tendons and muscles dealing with chronic and pathological pain for patients treated with conservative methods dealing with reflexive and centrifugal spastic muscles in the process of neurological rehabilitation acute and post-surgical sport injuries biological renewal Therapeutic effects of the whole-body cryotherapy:   highly beneficial...

DEKLARACJA ZGODNOŚCI / DECLARATION OF CONFORMITY KONFORMITÄTSERKLÄRUNG / DECLARATION DE CONFORMITÉ – DZ-KR-2010 – Nazwa i adres wytwórcy Name and address of the firm Name und Adresse der Firma Nom et adresse de l’entreprise PPHiU „KRIOSYSTEM” Sp. z o. o. ul. Muchoborska 18 54-424 Wrocław – PL Tel.: +48 (71) 349 00 20 Faks: +48 (71) 349 00 22 E-mail: [email protected] Deklaruje się z pełną odpowiedzialnością, że: We declare under our sole responsibility that Wir erklären in alleiniger Verantwortung, dass Nous déclarons sous notre propre responsabilité que Komora Kriogeniczna typ: KR-2010...