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Customized Medical Device Clean Room Assembly In 10K Environment OEM manufacturing

Categories Clean Room 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
clean room: clean room
environment: 10K environment
name: Clean Room Assembly
function: For medical
application: medical care / medical device
brand: JENITEK
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    Customized Medical Device Clean Room Assembly In 10K Environment OEM manufacturing

    Customized Medical Device Clean Room Assembly In 10K Environment OEM 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 products ranging from packaging and swabs to wound control and medical care, medical device must be safety. so production must meet the very highest of standards.


    For medical device solutions, durability, workmanship and cushioning are critical to guarantee perfect functionality.


    In a medical environment, the slightest product defect can expose stakeholders to potentially critical risks, be they patients, original equipment manufacturers, medical professionals or health care providers.


    In addition to factors such as tight tolerance, flow rates and wicking capabilities; cleanliness and aesthetics are of paramount importance.


    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 Aseptic package / Double packing / Vacuum package. Specifically configured to meet stringent packing validation requirements.


    Certificaton


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



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