Certifications
Certifications
Certification files, registration documents and product scope are evaluated according to the target market and project requirements.
Our China service office helps coordinate document lists and communication with the factory. Customers should confirm the applicable requirements before placing an order or launching a product.
Product specifications, manufacturing information and supporting files can be coordinated with the Korea factory.
Our China service office holds a Chinese Class III medical device registration certificate for relevant cooperation needs.
Registration, labeling and sales requirements differ by market and must be reviewed for each project.
We help organize the required documents for sampling, evaluation, registration and delivery.
Certification files and product approvals should be confirmed against the official documents and the intended sales market.
Request document support扫描二维码分享到微信