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SFDA IVDD Registration
| Price: | Contact for latest price |
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| Payment Terms: | N/A |
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Product Details
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| Specification: | N/A |
Packaging & Delivery
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Product Description
Currently in China, except the in vitro diagnostic reagents (IVDD) used for blood screening and adopting radioisotope labeling, other IVDD need to be managed as medical device (MD). IVDD is divided into three management categories according to their risk level. There are some special requirements during the IVDD registration in addition to the general regulations of medical device.
During the SFDA registration, class 2 and 3 IVDDs are required to conduct clinical trial in China. Osmunda has rich clinical resource and experience and would provide you with best all-round service.
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SUPPLIER PROFILE
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| Company: | Osmunda Medical Device Consulting Organization | ||
| City/State | Guangzhou, Guangdong | Country: |
China 
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| Business Type: | Export/Import - Trading Company | Established: | 2004 |
| Member Since: | 2011 | Contact Person | Osmunda |
SUPPLIER PROFILE
City/State/Country -
Guangzhou, Guangdong
China
Business Type -
Export/Import - Trading Company
Established -
2004
Member Since -
2011
Contact Person -
Osmunda