Medical Devices

NMPA Publishes 6 Regulatory Drafts Concerning Clinical Trials for Medical Devices and IVDs
NMPA Publishes 6 Regulatory Drafts Concerning Clinical Trials for Medical Devices and IVDs

The NMPA is currently soliciting public comments on the draft documents. The public consultation period is open until May 30, 2021.

March 13, 2026
NMPA Publishes 6 Regulatory Drafts Concerning Clinical Trials for Medical Devices and IVDs
China Adjusts Import Tariff of Medical Devices
China Adjusts Import Tariff of Medical Devices

883 commodities were announced under the MFN Rate of Duty whilst the import tariff rate on artificial heart valve, hearing aids, etc., reduced from 4% to 1%

March 29, 2022
China Adjusts Import Tariff of Medical Devices
Radio Frequency Beauty Devices will be regulated as Medical Devices Soon
Radio Frequency Beauty Devices will be regulated as Medical Devices Soon

The China NIFDC announced the technical guidelines (draft) for Radio Frequency beauty devices to be regulated as class II or class III medical devices.

March 29, 2022
Radio Frequency Beauty Devices will be regulated as Medical Devices Soon
Cisema Expands China Footprint with New Offices in Tianjin and Jinan
Cisema Expands China Footprint with New Offices in Tianjin and Jinan

Our testing engineers are specialized in EMC (Electro Magnetic Compatibility), electrical safety, physical and chemical property and biocompatibility tests.

March 29, 2022
Cisema Expands China Footprint with New Offices in Tianjin and Jinan
April 2021 China Regulatory Round-up for Medical Devices
April 2021 China Regulatory Round-up for Medical Devices

9 product categories have been reported by the NMPA for not meeting the standard requirements whilst 12 regulatory guidelines and drafts have been issued.

March 29, 2022
April 2021 China Regulatory Round-up for Medical Devices
What information needs to be provided when applying for a change in the packaging specifications of in vitro
What information needs to be provided when applying for a change in the packaging specifications of in vitro diagnostic reagents?

According to the announcement published by the Centre for Medical Device Evaluation) of the National Medical Products Administration on April 12, 2021...

March 29, 2022
What information needs to be provided when applying for a change in the packaging specifications of in vitro diagnostic reagents?
Working Procedures for Medical Device Quality Spot Inspections in China
Working Procedures for Medical Device Quality Spot Inspections in China

The announcement cover details of the working procedures and appendices for quality spot checks and inspection procedures for medical devices within China.

March 29, 2022
Working Procedures for Medical Device Quality Spot Inspections in China
New Details on Sampling Inspections of Medical Devices
New Details on Sampling Inspections of Medical Devices

Inspection work shall be carried out in accordance with the mandatory standards or product technical requirements for post-market activities in China.

March 29, 2022
New Details on Sampling Inspections of Medical Devices
First Hong Kong Medical Device Approved for Clinical Use in the Greater Bay Area
First Hong Kong Medical Device Approved for Clinical Use in the Greater Bay Area

The Guangdong MPA announced the first approved medical device arriving the University of Hong Kong – Shenzhen Hospital via the Greater Bay Area initiative.

March 29, 2022
First Hong Kong Medical Device Approved for Clinical Use in the Greater Bay Area
China Regulatory Round-up for Medical Devices in March 2021
China Regulatory Round-up for Medical Devices in March 2021

22 technical guidelines (draft) were issued in March 2021, and technical guidelines for products monitoring non-invasive blood / glucose will be drafted

March 29, 2022
China Regulatory Round-up for Medical Devices in March 2021
Update of Administrative Measures for the Clinical Use of Medical Devices
Update of Administrative Measures for the Clinical Use of Medical Devices

The NHC announced the implementation of The Administrative Measures for the Clinical Use of Medical Devices coming into force from March 1, 2021 onwards.

March 29, 2022
Update of Administrative Measures for the Clinical Use of Medical Devices
Guangdong’s Pilot Plan for Hong Kong Medical Devices to enter the China Greater Bay Area
Guangdong's Pilot Plan for Hong Kong Medical Devices to enter the China Greater Bay Area

The Guangdong MPA (Medical Products Administration) announced details about the pilot plan and the responsibilities of different departments involved.

March 29, 2022
Guangdong's Pilot Plan for Hong Kong Medical Devices to enter the China Greater Bay Area

Get in Touch with our Certifications team

And discover how we can support you in getting your products certified for China.

Request Proposal