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   August 4, 2022 5:19 pm Leave a Comment

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   Printed Circuit Boards, or PCBs, hold a variety of functions, sizes, and industrial applications. To add electrical components to the board, PCB assemblers utilize either surface or through-hole mounting methods. PGF Technology Group prides itself on offering both PCB techniques, with optional combinations of  SMT or through-hole technologies. By staying on the edge of technology, PGF continues to further integrate surface-mounting techniques to all applicable assemblies, saving both time and money. However, although the surface mounting techniques take precedent, PGF continues to provide authentic through-hole processes to best suit customer specifications. The presence of both techniques widens the PGF market, thus utilizing either process based on the most efficient solution.

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   The surface mounting PCB assembly method involves mounting electrical components onto the top of the printed circuit board. With surface mount technology (SMT), electrical components are installed in a simple and timely manner. The surface-mounting technique allows ample use of both sides of the board. Surface mounting SMT technologies automate the assembly process, increasing production speed while maintaining high-quality products. The Fuji and MyData machines are the two main types of machinery used to process PCBs.

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   • Allows for smaller PCB design, closely placed components
   • Compact and lightweight
   • Cost-effective with faster production time
   • More efficient designs with components aligned tighter together
   • More controlled manufacturing environment from automated machine technology

    

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   Through-hole mounting involves a pre-drilled hole to install and solder the electrical component to the printed circuit board. Typically used for large components, the through-hole method may also be utilized for attaching components determined incompatible with the surface mount technologies. Before SMT advanced automating technologies, the through-hole method was the main assembly practice to attach components to the board. While through-hole mounting is not as common, particularly military and aerospace industries utilize such methods to ensure durability in irregular conditions.

    

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   • With components attached through the board, such PCBs offer higher strength and reliability
   • Able to endure larger amounts of external physical stressors
   • Easily replaceable and thus desirable for various testing endeavors or prototyping projects
   • Ability to withstand higher heat capacities
   • The stronger bond between the board and the electrical components allows higher power capabilities

    

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   While offering both surface mounting and through-hole mounting techniques, PGF delivers high-quality products that meet all customer specifications promptly. Additionally, PGF offers X-Ray Evaluations and Ionograph Testing services to all customers, showcasing the company’s dedication to excellence. Learn more about the endless PGF advantages for all your PCB needs. Request a quote and experience all PGF premium services today!

   

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   December 10, 2021 8:52 pm Leave a Comment

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   When it comes to medical devices, no average or sub-par printed circuit board assembly (PCBA) is going to cut it! In this live-action game of Operation, the consequences are real, and the assembly is accountable.

   As a premier manufacturer of printed circuit boards, PGF Technology Group fully understands the importance of proper PCBA design for medical devices and systems. However, some may find the design process challenging since many factors must be considered. These factors include safety requirements, cleanliness standards, industry/application-specific regulations, and more. That’s why our team has put together the following guide, which goes over some of the key considerations to keep in mind when designing medical PCB assemblies.

    

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   Accuracy and precision are crucial to avoiding the buzzer. Many medical devices are designed to perform vital functions while living in or on the human body for extended periods, such as insulin pumps and pacemakers so that any malfunction can put the patient’s life at risk. That’s why manufacturers must design and build these products and their components carefully to ensure patient safety. PCBA manufacturers should consider the operational and environmental conditions (e.g., fluid exposure, temperature), their effect on the product, and the measures needed to combat those effects.

    

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   A clean workplace is a safe workplace. This saying is especially pertinent in the medical industry, where cleanliness can significantly affect the health and wellbeing of patients and the performance and lifespan of devices. That’s why PCBA manufacturers will often use materials that form surfaces that are easy to clean and disinfect and incorporate strict cleaning practices into production operations to remove any residues left behind from manufacturing processes. Additionally, according to the cleanliness of product clause in ISO 13485 Medical Devices — Quality Management Systems — Requirements for regulatory purposes, organizations need to document product cleanliness or contamination control requirements.

    

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   To properly play the game, you have to know the rules. In the medical industry, products are subject to numerous regulations outlining how they should be designed, manufactured, used, etc. Knowing, understanding, and following them is essential to the success of a product.

    

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   Firstly, one of the most critical regulations relevant to medical PCBAs and other electronics is ISO 13485, which establishes the requirements for quality management systems for companies involved in one or more of the lifecycle stages of a medical device or the supply of products. The 2016 update of the standard brought the requirements in line with those already mandated by the FDA.

   Companies can be certified to this standard, meaning their quality management system has been verified to meet its strict requirements. The requirements aim to ensure the production of high-quality medical products that are safe and effective, which is why many countries require medical device companies to attain certification. In addition, ISO 13485 certified companies benefit from higher customer satisfaction, greater customer trust, and better credibility.

    

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   Other specifications to consider are the IPC Class 3 Standards. Companies that meet these specifications value skill, constant improvement, and intense scrutiny. They know that a buzzer in the game signals a life or death scenario, so practices must be monitored and perfected.

    

   PGF Technology Group maintains the ISO 13485 compliance and IPC Class 3 Standards for any project connected to medical devices.

    

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   In addition to safety, manufacturers must keep in mind the usability of PCBAs. For example:

   • Is SMT or thru-hole assembly appropriate? Manufacturers should reference the specific design requirements from the client to ensure that they utilize the best method of assembly. This process may include prototypes to review board real estate and functionality.
   • How small is too small? While it can be tempting to go with the smallest PCBA design, a design that is too small can limit the complexity of your device. You need to ensure enough space to incorporate all components for a fully operational and reliable instrument.
   • What is the min/max amount of energy input? Determine the circuit’s energy to run during typical and peak operation.

    

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   Anyone who has built an IKEA item understands the pain caused by a hard-to-assemble project. Without clear-cut instructions and imagery to demonstrate design, the process can become prolonged. Medical PCBA designers can eliminate this pain by designing with assembly in mind; assemblers should not have trouble reaching and mating cables to connectors, soldering connections or placing other essential components. Additionally, the assembled product should be testable using various methods. Some examples include visual assessment, Solder Paste Inspection (SPI), X-ray scanning, In-Circuit Testing (ICT), and Automated Optical Inspection (AOI).

    

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   Want to learn more about the critical design considerations for medical PCB assembly? Ask the experts at PGF Technology Group! As an ISO 13485 certified company specializing in PCBA, we can answer or address any of your questions and concerns. Importantly, you can check out our eBook, Key Considerations for Medical PCB Assembly, to overview the vital considerations to keep in mind when designing and assembling medical PCBAs.

   At PGF Technology, we have the knowledge, experience, and certifications to deliver PCBA solutions that meet the most stringent specifications. Contact us or request a quote today if you want to partner with us for your medical PCBA needs.

   

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