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CE
CE means that Dio meets EU medical devices standard. With declaration of economy and CE mark, Dio duly exports to Europe per its medical device requirements.
CE
CE means that Dio meets EU medical devices standard. With declaration of economy and CE mark, Dio duly exports to Europe per its medical device requirements.
CE
CE means that Dio meets EU medical devices standard. With declaration of economy and CE mark, Dio duly exports to Europe per its medical device requirements.
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FDA
DIO received class 2, dental implant certificate from FDA which evaluates safety and validity of all medicines, foods and medical devices sold in the USA.
FDA
DIO received class 2, dental implant certificate from FDA which evaluates safety and validity of all medicines, foods and medical devices sold in the USA.
FDA
DIO received class 2, dental implant certificate from FDA which evaluates safety and validity of all medicines, foods and medical devices sold in the USA.
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KGMP
KGMP medical device manufacturing and quality management certificate.
KGMP
KGMP medical device manufacturing and quality management certificate.
KGMP
KGMP medical device manufacturing and quality management certificate.
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ISO 13485
DIO manufactures consistently excellent quality products per ISO 13485, international medical device quality management standard.
ISO 13485
DIO manufactures consistently excellent quality products per ISO 13485, international medical device quality management standard.
ISO 13485
DIO manufactures consistently excellent quality products per ISO 13485, international medical device quality management standard.
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CMDCAS ISO 13485
DIO received CMDCAS ISO 13485 certificate. Safety approval of medical device manufacturing system, from Health Canada.
CMDCAS ISO 13485
DIO received CMDCAS ISO 13485 certificate. Safety approval of medical device manufacturing system, from Health Canada.
CMDCAS ISO 13485
DIO received CMDCAS ISO 13485 certificate. Safety approval of medical device manufacturing system, from Health Canada.