Quality
As a manufacturer of medical devices it is our goal to provide innovative CPR products and services that meet or exceed our global customers needs and expectations.
The latest and global generations of LUCAS products; the pneumatic LUCAS 1 (V2) and the battery-operated LUCAS 2, are cleared for marketing in the US by a 510k, CE-marked in Europe, approved for sales in Japan, Canada, China and have several more international registrations.
Jolife AB, the manufacturer and developer of LUCAS, is certified according to ISO13485:2003, ISO 9001:2000 and Medical Device Directive 93/42.
Quality policy
To meet these requirements, our policy at Jolife is to:
• design and manufacture products that are consistently in compliance with customers’ and regulatory requirements.
• never compromise with safety or reliability of our products or services.
• use developments in science and feedback from our customers and markets as inputs for continuous improvement.
• identify and satisfy present and future demands of the customers, our most important partner, and
• present our products in an ethical manner.
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