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Sfda Registration - China

price: contact company for price

Base on the potential risks and intended use, medical

devices are divided into three management categories by SFDA of

China(State Food and Drug Administration). All medical devices need to

be registered according to Medical Device Registration Administration in

order to be sold and used in China. Different countries

have different regulations about medical devices, relying on the deep

understanding of various regulations and abundant practical experience,

Osmunda could help your products to be easily approved by SFDA and be

introduced into the Chinese market.

Sfda Registration

For any questions and needs please contact us below


Company Contact:


  • Phone: 862062321333

  • Address: 7th Floor, Jingui Business Building, No.982 Congyu, Guangzhou, China

  • Email: Email


Published date: September 7, 2012 -

  • Business Description: Osmunda Medical Device Consulting Organization

    (Guangzhou, Beijing, Shanghai, Suzhou, Shenzhen and Jinan) is the

    largest and most professional consulting company in the field of medical

    device in China. All Osmunda Consultant team members are from sizeable

    medical devices enterprises, well known notified bodies and testing

    organizations. We are well versed in global various medical device

    quality system certification and product registration, such as SFDA

    registration, QSR 820 system, FDA registration, ISO 13485 system, CE

    certification etc. Our service includes clean room design, clinical

    trail, third party audit, training of regulations and standards, etc.

    Our headquarters is in Guangzhou, and we have five branch offices (Beijing, Shanghai, Suzhou, Shenzhen, Jinan) which could provide high speed local services and communication. By far, Osmunda has successfully assisted nearly 1,200 domestic and foreign enterprises in achieving various medical devices registration and certification. We will be your trustful partner and your most professional guide.

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