MEDICAL HEAT TREAT

First Accreditation for MedAccred in Europe Awarded to Bodycote

Bodycote, the world’s largest heat treating services provider, is pleased to announce that its Derby, UK location is the first facility in Europe to earn the MedAccred accreditation underlining the high standards of quality achieved. The official approval was awarded on 7th of April 2016.

MedAccred, administered by Performance Review Institute (PRI), is an industry managed approach to ensuring critical manufacturing process quality throughout the medical device supply chain. It establishes stringent consensus audit criteria based on industry and specific OEM requirements that ensure compliance and quality. Adherence to these requirements leads to greater process discipline, operational efficiency and ongoing improvement which results in higher quality and performance.

Strategically located in the East Midlands, Bodycote Derby, which offers heat treatment and hot isostatic pressing (HIP) services, is fast becoming a centre of excellence serving the medical device and implants markets for the UK, Ireland and Europe. Bodycote continues to invest in new capacity and technology to support opportunities within the growing medical industry for classic heat treatment and HIP along with its Specialty Stainless Steel Processes (S3P) and Ion Implantation services in Europe. For Bodycote, the benefits of MedAccred to the supplier are evident. The process provides for consistent and standardised critical process audits which result in fewer redundant onsite audits by multiple OEMs and first tier customers. The MedAccred certification should reinforce customer confidence in Bodycote as a premier quality provider of heat treating.

Joe Pinto, Executive Vice President and Chief Operating Officer of the Performance Review Institute, the organisation which administers the MedAccred program on behalf of the medical device industry, sent his congratulations to the team at the Bodycote Derby facility: “We are delighted that Bodycote has the honour of becoming the first company to receive an accreditation from MedAccred in Europe. To be the first in anything demonstrates a high level of foresight and commitment to a long term strategy. The MedAccred audit is challenging and in achieving accredited status, Bodycote’s Derby facility has proven it has the capability to meet and exceed the requirements of its medical customers. The entire team should be proud of their success.”

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NIST, Partners Create Standard to Improve Sustainable Manufacturing

BOTW-50w  Source:  Today’s Medical Developments

“According to the U.S. Energy Information Administration, manufacturing accounts for one-fifth of the annual energy consumption in the United States – approximately 21 quintillion joules (20 quadrillion BTU) or equivalent to 3.6 billion barrels of crude oil. To reduce this staggering amount and improve sustainability, manufacturers need to accurately measure and evaluate consumption of energy and materials, as well as environmental impacts, at each step in the life cycles of their products.”

Read More:  NIST, Partners Create Standard to Improve Sustainable Manufacturing

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3D Printing, Ultrasonic Milling Medical Orthopedic Devices

BOTW-50w  Source:  Today’s Medical Developments

“Our Austofix product design engineers, working with IPAS, were able to innovate within a flexible design and manufacturing process. This environment was key to our ability to take the prototype to market within such a short timeframe,” he said. “There are key components of the plate manufactured using 3D printing, this enabled us to create a complex design without the costs associated with traditional manufacturing. It also enabled us to bring the device to market quickly.”

Austofix has a number of products including a range of stainless steel and titanium surgical nails, which it exports to the Middle East and China.”

Read More:  3D Printing, Ultrasonic Milling Medical Orthopedic Devices

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FDA Has Important New Views on 3-D Printed Devices

BOTW-50w Source:  MPMN Medtec Pulse

The FDA has released “leapfrog” draft guidance for the rapidly evolving world of 3-D printed medical devices.

The agency based the guidance on input from device manufacturers, 3-D printing companies, and academics who testified at a 2014 hearing. The document covers device design, manufacturing, and design testing. For the purposes of the draft, FDA identified four main types of 3-D printing—powder fusion, stereolithography, fused filament fabrication, and liquid-based extrusion.

Manufacturers would have to clearly identify every step in the 3-D printing process, and might need to submit a “high-level summary of each critical manufacturing process step,” the guidance says. They would also have to document each step’s risk, and describe how they would mitigate those risks.

Read More:  FDA has Important New Views on 3-D Printed Devices

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7 Recent Medical Device Failures Catching FDA’s Eye

BOTW-50w Source:  QMED – Qualified Suppliers to the Medical Device Industry

“The FDA last month designated a Medline Industries guidewires recall as Class I.

The Medline guidewire is identified as the ACME Monaco Guidewire .035×150 3MMJ TCFC item number 88241, with affected products distributed between March 2013 and August 2013.

The guidewire is used in various surgical convenience kits assembled and marketed by Medline Industries. It is meant to fit inside a percutaneous catheter for the purpose of directing the catheter through a blood vessel.

The guidewires in question, however, have the potential for the coating to flake off of the wire, according to the FDA.”

Read More: 7 Recent Medical Device Failures Catching FDA’s Eye

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Plastics and Metals Team Up in Medical Device Apps

BOTW-50w Source:  MPMN Medtec Pulse

“… to be able to deliver devices with ever-increasing performance levels, medical device manufacturers continue to face many design challenges and requirements. Propelling these requirements is the unrelenting trend toward minimally invasive procedures, requiring smaller and smaller devices made from a range of microcomponents, and the trend toward increasing medical device connectivity. As a result, there is a growing need to unite plastics and such metals as stainless steel, although they used to be fierce competitors.”

Read More: Plastics and Metals Team Up in Medical Device Apps

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Stryker’s Spine Division to Debut 3D Printed Tritanium Posterior Lumbar Cage Spinal Implant

BOTW-50w Source:  3D Print.com

“Stryker’s proprietary Tritanium technology has now been applied to spinal implants designed to encourage healthy regrowth of the bone tissue, and to reduce any strain or damage caused by being implanted. The Tritanium Posterior Lumbar (PL) Cage is a 3D printed intervertebral body fusion device that was developed to help patients dealing with lumbar spinal fixation due to ongoing back problems brought on by degenerative disc disease.”

Read More:  Stryker’s Spine Division to Debut 3D Printed Tritanium Posterior Lumbar Cage Spinal Implant

Stryker’s Spine Division to Debut 3D Printed Tritanium Posterior Lumbar Cage Spinal Implant Read More »

Solar Atmospheres Receives First Reaccreditation from MedAccred

Solar Atmospheres, Inc. has announced that it has become the first company to receive MedAccred critical process reaccreditation.  Furthermore, Solar Atmospheres, Inc. successfully expanded its scope of accreditation to include Hardness Testing and Metallography & Microindentation Hardness.  MedAccred is an industry-managed critical process supply chain oversight program which was developed by leading medical device companies to improve device quality and most importantly enhance patient safety.

The effort to establish MedAccred began in 2010 when the Performance Review Institute (PRI) was asked to consider the development of a Nadcap-style special process supplier accreditation program for the medical device industry.  An industry roundtable was organized and convened in 2012 among interested medical device companies and PRI.  Following this roundtable meeting, briefings were held with the FDA Center for Devices and Radiological Health’s (CDRH) Office of Compliance and the FDA’s Office of Global Operations within the Office of the Commissioner. The program purpose and scope was discussed, along with the results of proof of concept audits which were conducted to demonstrate the program’s viability. The FDA provided positive feedback and strong encouragement to pursue the development of the program.

By 2014, several critical process Task Groups were operating on a formal basis, program documents were drafted, circulated and approved by the executives of the participating companies and audit criteria had been published in several critical process areas.  Solar Atmospheres, Inc. committed to hosting the first MedAccred audit.

In early 2015 the first MedAccred critical process accreditation was issued to Solar Atmospheres Inc. for Heat Treating.

Today’s functioning critical process Task Groups include Cable & Wire Harnesses, Heat Treating, Plastics Injection Molding, Printed Circuit Board Assemblies, Sterilization and Welding.  The industry managed task groups develop audit criteria, conduct audits, and award MedAccred Critical Process Accreditations to leading suppliers at all tiers in the Medical Device Supply Chain.  Many companies are seeking MedAccred Accreditation to demonstrate their commitment to quality and patient safety. Future MedAccred Task Groups under consideration for development include Material Testing Laboratories, Assemblies, PCBs, Batteries, Chemical Processing, NDT, Cleaning, Coating, Optics, Packaging, etc.  Active OEM and Contract Manufacturer participants include: Johnson & Johnson, Philips, Stryker, GE Healthcare, Medtronic, NYPRO Jabil, Steris, etc.  The list of participating suppliers is growing steadily.

Joe Pinto, Executive Vice President and Chief Operating Officer of PRI explained the significance of Solar Atmospheres’ accomplishment: “Gaining a critical process accreditation from MedAccred is recognition of a company’s commitment to quality and the high standards of critical process manufacturing which they maintain.  The successful completion of a reaccreditation audit is a clear indication that a company is able to consistently uphold those extremely high standards over an extended period of time.   I would like to congratulate the whole team at Solar Atmospheres on this important achievement.”

Solar Atmospheres Receives First Reaccreditation from MedAccred Read More »

Element Launches World-Leading Material Testing, PQT Facility

Following significant capex investment, Element Materials Technology has launched its newly expanded and upgraded Cincinnati, Ohio, facility, as one of the largest independent materials testing and product qualification testing (PQT) service facilities in the U.S. The former-Accutek location has expanded to 62,000ft2 and now provides specialist testing to both the aerospace and medical device sectors and houses three of Element’s Global Centers of Technical Excellence delivering critical testing services to these sectors.

Charles Noall, president and CEO of Element, comments: “Our investment at Element Cincinnati marks a significant step towards securing our position as the strategic partner of choice for our clients in the aerospace and medical device industries. We are committed to developing Centers of Technical Excellence across our global platform, allowing us to deliver market-leading technical expertise where needed by our partners, from aerospace primes to leading medical device manufacturers.”

Element Cincinnati is a world-leading ceramic matrix composite (CMC) Center of Technical Excellence, that is equipped with market-leading environmental controls, high temperature facilities (up to 2,400°F) and doubled capacity in CMC testing, to support its major clients in the development of the next generation of aero engines. The laboratory also houses the Element Group’s Center of Technical Excellence in low-cycle fatigue (LCF) testing, which tests aerospace forgings for airframers and their supply chain partners. Finally, the laboratory also contains the group’s medical device testing center of Technical Excellence that offers a comprehensive range of 21 test methods including accelerated aging testing capabilities and mechanical testing for physiological studies for new spine, knee and hip wear simulator evaluations.

Rick Sluiters, Element’s executive vice president, aerospace, comments: “Our investment at Element Cincinnati allows us to act as a strategic partner to primes and OEMs working at the forefront of CMCs for the aerospace sector. The CMC Center of Technical Excellence provides testing services to respond to the industry’s most demanding challenges through the laboratory’s market-leading environmental controls. The increase in quality of environmental controls also gives us a very tight tolerance, allowing for highly accurate measurement of straining of CMCs.

“The investment also enhances the location’s medical device capabilities, with the mechanical, biological and related testing services allowing us to act as a full-service testing provider for clients. Element Cincinnati is a leading center for Medical Device testing and its newly expanded scope of accreditation underlines our commitment to acting in strategic partnership with key clients.”

Element Cincinnati is Nadcap and ISO accredited, as well as having an impressive range of Original Equipment Manufacturer (OEM) approvals, including GE Aviation, Snecma, MTU, Honeywell, Kawasaki Heavy Industries, Rolls-Royce (Germany, U.K., and U.S.), Pratt & Whitney, and Bell Helicopter.

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Heat Treating Opportunities Available in Medical Industry

BOTW-62w Source: Q1 Productions

Executive Vice President & Chief Operating Officer
Performance Review Institute (PRI)

“2016 is going to be a milestone year in terms of MedAccred’s development. The program has established itself in 6 critical process areas (PCBAs, Cable & Wire Harnesses, Heat Treating, Sterilization, Plastics and Welding) and numerous companies are now stepping forward to participate in the audit process and gain accreditation.”

Read More: 3rd Annual Medical Device Supplier Quality Conference: Speaker Interview – Joseph Pinto/Performance Review Institute

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