U.S. FDA REGISTRATION 2024
Renewal of FDA Medical Device registration. We have just received our new certificate from Registrar Corp who has renewed our FDA Medical Device registration with no comments. &nbs… Continue reading
Renewal of FDA Medical Device registration. We have just received our new certificate from Registrar Corp who has renewed our FDA Medical Device registration with no comments. &nbs… Continue reading
Radiotherapy has seen rapid advancements in the recent past, and Candor Aps is at the forefront of crafting tools and equipment that promise to elevate the quality of care given to patients. Today, we’re thrilled to introduce two of our latest products that seamlessly blend technology, design, and user-friendliness to ensure enhanced patient comfort and … Continue reading
Renewal of ISO certificate after annual audit by EXVERITAS on our quality management system. We have just received our new certificate after a successful audit from EXVERITAS of our quality management system with no comments. &nbs… Continue reading
For english see below the danish Pressemeddelelse Generationsskifte startet i SMEL industry Aps og Candor Aps, Sandager I begyndelsen af april blev de første formelle skridt taget til generationsskifte i de 2 Sandager virksomheder, SMEL Industry ApS og Candor ApS. Virksomhederne blev startet af Erik Langelund og hustru Helle tilbage i 1990 og 2007. Generationsskiftet … Continue reading
ESTRO 2022 – Europe’s largest industrial exhibition in radiation oncology You will find Candor Denmark at booth 350 in Hall E ESTRO 2022 will thies year optimise the contributions from submitted abstracts. Sessions with highlights of proffered papers will take place in a plenary setting, offering maximum visibility to your work. Furthermore, we will give … Continue reading
We had last week external audit of EXVERITAS on our quality management system ISO9001:2015. We were praised for our active use and expansion since the last audit. Today we have just received our new certificate… Continue reading
We are very proud to announce that Candor have been approved as a 3 part manufacture to VARIAN. More information about this news will follow soon… Continue reading
Candor has by 20. Of may 2020 registered all their products regarding MDR/UDI registration systems. This is made according to: EN ISO 14971:2009 Medical devices – Application of risk EN 62366-1:2017 Medical devices – Part: Application of usability engineering EN ISO 15223-2:2010 Medical … Continue reading
ExVeritas has the 21. oktober 2020 made a re Certification of Candor’s quality system ISO 9001:2015 The audit had no non conforming issues… Continue reading
Candor plans to design and produce a “S-Board” suitable for S-MASK systems and will fit all commercially sold patient tabletops. Are you interested? – please send os a message here… Continue reading