CUSTOMER SERVICE
Instructions for use
Instructions for use
In compliance with article 13.6 of annex I of European Directive 93/42/EEC, all Microdent products are supplied with the information needed for correct and safe product use. The bone expansion and condensation system is supplied with the necessary information for the correct use of the product in compliance with article 10; point 11 and section 23 of annex I of regulation MDR (EU) 2017/745.
Instruction for use: Medical Device legally marketed in the U.S.
Implants
- Packaging for Microdent Implants
- Packaging for Microdent Implants with multifunction abutment
- Packaging for Microdent Implants without implant-holder
- External Connection Microdent System Implants
- External Connection Microdent System Pro short Implants
- External Connection Microdent System V (conical) Implants
- External Connection Microdent Universal Implants
- External Connection Microdent Universal V (conical) Implants
- Internal Connection Microdent Trylogic Implants
- Internal Connection Microdent Trylogic V (conical) Implants
- Internal Connection Microdent Genius Implants
- Internal Connection Microdent Genius V (conical) Implants
- Internal Connection Microdent Genius Implants with multifunction abutment
- Internal Connection Microdent Genius V (conical) Implants with multifunction abutment
- Internal Connection Microdent Ektos Implants
- Internal Connection Microdent Ektos Pro short Implants
- Internal Connection Microdent Ektos V (conical) Implants
- Provisional Microdent Implants
- Microdent Orthodontics MicroImplants
