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Medical device assembly for OEM contract manufacturing

Categories Medical Device Assembly
Place of Origin: China
Brand Name: OEM
MOQ: 1
Price: discuss personally
Packaging Details: Aseptic package / Double package / Vacuum package
Delivery Time: According to contract request
Payment Terms: T/T
Supply Ability: According to products feature
name: clean room assembly
function: medical
application: for hospitals
OEM accept: Yes
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    • Company Profile

    Medical device assembly for OEM contract manufacturing

    Medical device assemble for OEM contract manufacturing


    Quick Details:

    Material:Titanium,platinum,stainless steel, brass, plastics,
    processing range:According to customer’s request
    Function:For medical
    Certificate :ISO 9001/ISO 13485 / ISO 14001 / OHSAS 18001

    Description

    For medical equipment suppliers, To satisfy stringent safety regulations, it is essential that medical components perform precisely and consistently to product-specific requirements.


    Suzhou Jenitek currently manufactures products for interventional and implantable devices. and includes a Class 100,000 Clean Room, with capabilities up to class 10,000, and certified Class 100 Laminar Flow Hoods. 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.


    Quality Assurance

    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.


    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 validation requirements.


    Certificaton

    · ISO 9001:2008Certified
    · ISO 13485:2012Certified
    · ISO 14001:2004Certified
    · OHSAS 18001Certified
    ·

    Quality Medical device assembly for OEM contract manufacturing for sale
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