Precious metal device converted into medical parts
|processing range:||According to customer’s request|
|Certificate :||ISO 9001/ISO 13485 / ISO 14001 / OHSAS 18001|
Our implement processing is to use special post-processing
technology and non-contact measuring methods to inspect them.
Regular audits and factory inspections by CSA ensure our quality
system operates at the level of performance required to
consistently produce high quality.
Often times our micro machined parts reach the smallest limit and
we hold tolerances to meet customer requirement.
And our manufacturing process applies strict controls to deliver
quality products on schedule.
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. Sealer and testing
equipment specifically configured to meet stringent packing
|· 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|