Arrotek

Case Study: Design & Manufacture of a Novel Injection Catheter

Medical device company SmartWise Sweden AB selected Arrotek as its design partner for the development of a novel endovascular injection catheter. It is an ongoing project, but this case study outlines the work we have done with the SmartWise team to date, developing the product, optimising the design, and providing support as it achieved FDA Case Study: Design & Manufacture of a Novel Injection Catheter

How Arrotek Adds Value to Your Medical Device Start-Up Company

Your medical device start-up has fantastic potential, but it’s essential to make the right decisions today to maximise its value in the future and make it attractive to investors and/or potential buyers. That means finding the right partners to progress your idea. Running a start-up medical device company is an exciting but often very busy How Arrotek Adds Value to Your Medical Device Start-Up Company

Medical Device Design Services – Support from Concept to Full-Scale Production

By Richard McLoughlin Bringing a new medical device product to market is an intensive and extensive process, so it’s important you get the right support. The best approach is to work with a partner that offers a complete service offering, with end-to-end support from the concept development stage through to full-scale manufacturing. At Arrotek, we Medical Device Design Services – Support from Concept to Full-Scale Production

Arrotek Shortlisted for MedTech Company of the Year 2022

Arrotek has been named as one of two finalists for the MedTech Company of the Year Award at the Irish MedTech Awards 2022. The Irish MedTech Awards are run by the Irish MedTech Association, Enterprise Ireland, and IDA Ireland. The MedTech Company of the Year Award is one of nine awards that will be announced Arrotek Shortlisted for MedTech Company of the Year 2022

Arrotek Medical Opens US Office

Arrotek Medical has opened a new office in Massachusetts, USA. The office is part of our strategic growth plans and will enhance the service we offer to our growing client base in the US and Canada. Richard McLoughlin, Sales and Marketing Manager at Arrotek, said: “The United States has been an important market for us Arrotek Medical Opens US Office

Choosing the Right Fine Needle Aspiration or Fine Needle Biopsy Device

By Paula Johnson While fine needle aspiration (FNA) and fine needle biopsy (FNB) are common procedures for the diagnosis of cancer, there is no specific device option that is the best choice in all situations. In fact, there is a large range of design and feature options available in both the FNA and FNB categories Choosing the Right Fine Needle Aspiration or Fine Needle Biopsy Device

Three-Phase Design Transfer Process to Prepare a Design for Manufacturing

Design transfer is a phrase that describes the activities and processes that introduce a medical device design to production. Effective design transfer is required by regulators but it also keeps manufacturing costs under control and ensures production milestones and deadlines are met. Furthermore, effective design transfer can reduce time to market and improve product quality. What Three-Phase Design Transfer Process to Prepare a Design for Manufacturing

Tailored Support for Your Medical Device Start-Up Company

There is a problem in the medical device industry and as a start-up company, it will be a problem that you may already be familiar with. You need support for your project, whether you are at the concept and prototyping stage or are further along on the research and development journey. However, all too often, Tailored Support for Your Medical Device Start-Up Company

Arrotek’s Modular Approach to Medical Device Design and Development Services

Our modular approach to the delivery of medical device design and development services means we can help with whatever level of support you need, whatever expertise you need, and wherever you are in the development process. While there are similarities across all medical device design and development projects, our experience at Arrotek is that every Arrotek’s Modular Approach to Medical Device Design and Development Services

Bottlenecks, Timelines, and Complexity: Overcoming EU MDR Challenges

It is now over a year since the new EU Medical Device Regulation (MDR) came into effect. Whether you are an early-stage start-up, a company further advanced in your start-up journey, or an established medical device company, what are the current realities of EU MDR compliance? The fact is, there are challenges that will impact Bottlenecks, Timelines, and Complexity: Overcoming EU MDR Challenges