Myriad is registered with the FDA as a Contract Device Manufacturer. Our registration number is 1225984. Our facility is cGMP compliant under 21CFR 820.
Myriad is also ISO 13485: 2016 certified, as a contract manufacturer of fiber optic imaging and illumination devices for the medical device industry. This certificate also covers our machine shop services.
Myriad’s quality system has been audited and found compliant to; ISO 9001, and the Japanese standard: MHLW Ministerial Ordinance No. 169, 2004.
Myriad fiber Imaging warranties its products, craftsmanship and materials, for six months from the date of manufacture.
Dedicated to meet or exceed our customer’s specification
when developing and manufacturing products.