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Because of a very tough market for medical devices the company has adapted its activities in a comprehensive manner to the European requirements. The main document which is regulating the obligations of the manufacturer and distributor of medical devices is Medical Devices Act of 26 April 2004. Act in the wake of the EU Directive 93/42 EEC on the manufacturer imposes a number of fundamental obligations to make the medical device market:
- Assess the product in conformity with EU requirements,
- Issue a Declaration of Conformity with the essential requirements of EEC Directive 93/42 and CE marking of products,
- Implement a continuous monitoring of the production, distribution, and develop procedures for dealing with nonconforming product
- Registering a product in the registry of medical devices, and those responsible for putting them into circulation.

The meaning of the law firm is a producer who has marketed its own devices or an authorized representative of the other manufacturers. One-time production of our clothing is disposable medical device selected in accordance with the requirements of the Act as class: not sterile.

Our products, as well as all raw materials used to produce them have a favorable opinion of the Institute of Medicine and the National Institute of Hygiene.

Our business is insured for liability is a liability. Indemnity Insurance for the product purchased by the equivalent of 50 thousand. EUR relieve the owner from any claims for compensation.

Individual packaging of the product contains all the necessary information: date of manufacture and expiry date, bar code product, manufacturer, CE marking, and instructions for use.