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What you'll learn:
Are there differences in the requirements of the Medical Device Regulation (MDR) for 3D-printed implants compared to traditionally manufactured implants?
What is the difference between Custom Made and Patient Specific?
What steps need to be taken to obtain CE marking for 3D-printed medical devices under the MDR?
Does the printed device for my implant also need to undergo biocompatibility evaluation?
Must a material certified by the manufacturer be re-evaluated for its biocompatibility?
Material with intended purpose vs. material without intended purpose. Does it provide any facilitation?
How does the MDR affect the liability of manufacturers of 3D-printed medical devices? 3D printing manufacturers vs. end users
Are there guidelines specifically developed for 3D printing in the medical field?
Are there specific requirements for training personnel involved in the manufacturing or use of 3D-printed medical devices under the MDR?
How can one ensure that 3D-printed medical devices comply with the quality and safety standards of the MDR?
What role does traceability play in the manufacturing of 3D-printed medical devices under the MDR? Is an Excel sheet sufficient?
Medical Expert & Lead Auditor AM at TÜV SÜD
Director Global Strategic Business Development Orthopedics at TÜV SÜD
Medical Market Development Manager at Formlabs
Co-founder and CEO at Formlabs
9:09 |
Adam explains the “Low Force” in Low Force Stereolithography (LFS) |
13:31 |
Deep dive into the light processing unit of the Form 3 |
25:19 |
Choosing a material with the Formlabs workflow |
31:00 |
Faris shows how to use the Form 3 |
40:16 |
Adam shows how to remove light touch supports |
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