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|Name:||Deep Hole Drilling Electrical Discharge Machining Cutting||Applications:||Hospitals|
EDM cutting and deep hole drilling for OEM contract manufacturing
|Min. cutting width:||0.020 mm|
|Accuracy :||+/- 0.005 mm|
|Materail||Full series of stainless steel, Platinum-Iridium alloy, Ni & Ti alloy, Copper|
The main purpose of spark machining is to process die and parts with complex shaped hole and cavity. During edm, tool electrode and workpiece are respectively connected to the two poles of the pulse power supply and immersed in the working fluid, or the working fluid is charged into the discharge gap.
Through clearance control tool electrode to the workpiece feeding automatic control system, when the gap reached a certain distance between the two electrodes, a pulse voltage applied on two electrodes will be working liquid breakdown, produce the spark discharge. With thousands of pulses of electricity per second, more metals can be corroded and removed with a certain rate of productivity.
Jenitek is committed to supplying products and services that meet the needs of customers, comply with statutory and regulatory requirements, increase customer satisfaction and maintain the effectiveness of the quality management systems through continuous improvement in products, processes and services.
Jenitek's quality management system has been certified ISO 13485:2012 and ISO 9001:2008 in order to fulfill each of our customers' specific requirements. FDA's QSR 21 CFR PART 820 and EU MDD 93/42 EEC certifications are in process.
We have a thorough quality system including four levels of documentation including manuals, procedures, work instructions and records. According to system documentation and processes, our quality activities such as production, inspection, product development (NPI), process validation, supplier chain control, and continuous improvement are controlled. This means we can deliver precision, performance and safety products and services to our customers around the world.
6 Sigma Quality Team The Jenitek quality team understands these system standards are not only the foundation of quality management but also paramount to the importance of our medical products, customers and product development, production, and improvement process. We have extensive experience with quality management and use a range of methods and tools, including IQ/OQ/PQ, FMEA, PFMEA, and Design of Experiments (DoE) to support in product development and improvement processes.
Packing and Tracing
Products with validated sterile packing. Specifically configured to meet stringent packing validation requirements.
ISO 9001:2008 Certified
ISO 13485:2012 Certified
ISO 14001:2004 Certified
OHSAS 18001 Certified
FDA 21CFR 820 In-Process
EU MDD 93/43 In-Process
ISO 14971 2004 Compliance