Inquiry

Welcome to the MDSS Inquiry page: Please use this form to detail the areas of your interest, so that we may reply with all the information you need to decide on MDSS's ability to help your company attain its needs:

Name

Address

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Areas of Interest

Conformity Assessment Procedures for CE
Certification Device Classification
Technical Files for CE Certification
Labeling for CE
Self-Certification Procedure (Available ONLY for CLASS I devices
Notified Body selection
Product Vigilance, within the EU
Medical Device Reporting (MDRs), within the EU
More information regarding ‘EU Authorized Representative / Authorized Address’
Quotation for services as a 'EU Authorized Representative /Authorized Address
National Registration
Consulting

ADDITIONAL QUERIES, REQUESTS AND/OR COMMENTS