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Medtech Manufacturing Cleaning and Sterilization Validation

Medtech Manufacturing Cleaning and Sterilization Validation

Medtech Manufacturing Cleaning and Sterilization Validation—A Medtech Makers Q&A Ensuring components remain residue-free and are properly sterilized are critical tasks for medical device firms. by.

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How Industrial CT Scanning Improves Additive Manufacturing

How Industrial CT Scanning Improves Additive Manufacturing

How Industrial CT Scanning Improves Additive Manufacturing OEMs are seeking manufacturing partners who can leverage multiple technologies to design and fabricate the instruments for orthopedic.

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Cleaning Coupon Increases Efficiency and Ensures Quality for AM Processes at rms Company

Cleaning Coupon Increases Efficiency and Ensures Quality for AM Processes at rms Company

One of the most well-known benefits of additive manufacturing (AM) is the ability to integrate elaborate surface technologies. These technologies, such as lattices and gyroids, allow for improved.

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Women in Medtech: Angie Hillyard

Women in Medtech: Angie Hillyard

Women in Medtech 2021: Angie Hillyard, Spectralytics Engineering Director by Sponsored Content, Medical Device & Outsourcing | October 12, 2021 Angie Hillyard, Engineering Director at Cretex Medical,.

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From Powder to Package: Identifying the Right AM Suppliers

From Powder to Package: Identifying the Right AM Suppliers

From Powder to Package: Identifying the Right AM Suppliers Medical device contract manufacturer rms Company watched additive manufacturing develop and evolve, and ultimately saw an opportunity to.

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Medtronic Launches Proprietary Surface Technology on AM Devices

Medtronic Launches Proprietary Surface Technology on AM Devices

Medtronic Launches Proprietary Surface Technology on AM Devices Medtronic became interested in additive manufacturing (AM) to extend its innovation, unlocking advantages exclusive to the technology..

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Meier Featured in SciTech Internship Program

Meier Featured in SciTech Internship Program

Our precision metal stamping team (formerly Meier Tool & Engineering) was recently featured in an article by SciTech MN titled Internship Feature: Meier Tool and Engineering. The article focused on.

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UDI Regulation Compliance: First Phase Guidance Document Issued

UDI Regulation Compliance: First Phase Guidance Document Issued

Compliance to the UDI regulation includes the FDA public database, GUDID. The first phase of the Global Unique Device Identification Database (GUDID): Guidance for Industry document is now available..

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DuPont Tyvek Transition Update

DuPont Tyvek Transition Update

DuPont Tyvek Transition Update DuPont is transitioning Tyvek® 1073B and Tyvek® 1059B to manufacturing lines that use the latest flash-spinning technology to help ensure greater continuity and.

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UDI Rule Announced

UDI Rule Announced

Unique Device Identification (UDI) Final Rule was announced by the FDA on September 20, 2013. The rule was published in the Code of Federal Regulations as of September 24, 2013. Implementation for.

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