The SMARTFLOW 2020 is a compact, cell-based selective soldering system with a base area of less than 2, 5 m². The acquisition of a 2nd SMARTFLOW 2020 system by Realtime provides another level of flexibility and supports both rapid product changeover for various high-mix, high-quality, low volume builds as well as offering increased throughput and maintaining consistency when both machines are required to support the same product range in larger batch builds.
Selective Soldering System SMARTFLOW is one of the 1st platforms to use the ERSASOFT 5 operating system.
It offers a very stable, intuitive and flexible user interface which facilitates live process monitoring, as well as the ability, adjust and optimize program process parameters while the machine is running.
With the ability to quickly change the solder bath in the SMARTFLOW 2020 Realtime also has the flexibility to change the Alloy it uses in the Selective Soldering process to satisfy both customer and regulatory requirements in a matter of minutes.
With the supply of high-quality Nitrogen available from Realtime’s on-site N2 generation plant readily available the installation of the new SMARTFLOW was completed and available to production within a day.
The Ersa SMARTFLOW 2020 utilizes the same software platform as well as the Wear-Free Electromagnetic Induction Pump and Fluxer Technology used on the larger fully automatic inline machines from ERSA. This, aligned with excellent quality produced and the high Overall Operational Efficiency seen from the SMARTFLOW 2020 by Realtime over the last year has made the equipment selection process for Realtime in choosing the 2nd system an easy one.
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This demonstrates Realtime’s ability to provide medical equipment and related services that consistently meet customer requirements and regulatory requirements applicable to medical equipment and related services.
ISO 13485:2012 details specific requirements for a quality management system where organizations need to demonstrate their ability to provide medical equipment and related services that consistently meet customer requirements and regulatory requirements applicable to medical equipment and related services. The ISO 13485:2012 standard is globally recognized as the best quality practices from organizations within the medical device industry.
Registration was a goal for Realtime, although it was recognized that the pursuit of quality provides benefits well in excess of gaining registration. Robust, quality-imbued processes add immense value to the development, manufacture, distribution and to both the internal and external customer.
ISO 13485:2012 helps Realtime Technologies to provide a structure for implementation of requirements. It ensures the achievement of these planned results and the maintenance and effectiveness of those processes in relation to the customer, internal quality and regulatory requirements. Due to the nature of the medical equipment, safety is one of the principal requirements.
Realtime Technologies is an electronics contract manufacturer and services provider. With a reputation for quality and flexibility, we design and build products for Secure Payment Systems, Aerospace, Automotive, and Medical sectors. Comprising of facilities in Ireland, Czech Republic, US, Slovakia, and offices in the Far East and South America, we provide the most cost-effective and efficient route to bring your product onto the global market. From single item prototypes to medium and high volume quantities, Realtime can deliver the trusted experience and expertise needed to drive your product development and business growth forward.