For a given reason, we would like to point out that the use of Cryoalfa equipment is expressly permitted only with, original accessories and consumables, made by or authorized by the manufacturer.
The Cryoalfa products are labeled.
The existing CE certificates and Medical Device Directives IIA under which the products are registered are legally binding documents and the regulations in them must be followed. At the moment our equipment is used with third part consumables and accessories, above CE-certificates and Medical Device Directives IIA cease to be valid. This implies that the product not longer is allowed to be used for intended purpose.
Failure to follow existing regulations is an unlawful act of the distribution company and the user. The manufacturer will not assume any responsibility for the device’s safety or functional ability in the event of improper handling or usage contrary to the intended purpose. In the event of unauthorized alterations/modifications, both the warranty claim and the conformity will expire.
It also voids all warranty claims for any material and / or personal injury resulting from these unlawful distribution, use and application. Cryoalfa explicitly disclaims any liability for Cryoalfa devices that are sold and used in connection with these third-party consumables or accessories.
Note: Currently is on the market a Cryoalfa- device with capsules with 23.5 g N2O fill weight that are not of Cryoalfa origin. Cryoalfa capsules (gas containers) are characterized by tamper-proof Cryoalfa original labels with consecutive single registration number.
