Application Forms

(EU) 2017/745 Medical Device Regulation

(EU) 2017/745 Medical Device Regulation
Product Information (EU) 2017/745 Medical Device Regulation
MDR Article 117 Application Form (NOTE: This application form should only be filled out by manufacturers who request a Notified Body opinion within the scope of Article 117.) (EU) 2017/745 Medical Device Regulation

ISO 13485 Medical Devices- Quality Management System Certification Application Form-Turkish Accreditation Agency

Product Certification (TS EN ISO/ IEC 17065)-Turkish Accreditation Agency

Machine Safety Directive Product Certification (TS EN ISO/ IEC 17065)-Turkish Accreditation Agency
Construction Products Regulation Product Certification (TS EN ISO/ IEC 17065)-Turkish Accreditation Agency
Lift Directive Product Certification (TS EN ISO/ IEC 17065)-Turkish Accreditation Agency

Laboratory (TS EN ISO/IEC 17025) – Turkish Accreditation Agency

Training Application Form

UDEM Systems & Product Certification Services

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