CFDA Issued Six New Guidelines

Registration guideline

Scope of application

Issued date

Blood and blood component storage bag Registration Guideline.

全血及血液成分贮存袋注册技术审查指导原则.pdf

This guideline can apply to blood bag that managed as medical devices as a reference for the non-clinical evaluation part registration dossiers preparation and product technical review.

01/10/2018

Disposable infusion pump (non-electric drive) Registration Guideline.

一次性使用输注泵(非电驱动)注册技术审查指导原则.pdf

This guideline can apply to disposable infusion pump (non-electric drive) as a reference for registration dossiers preparation and product technical review.

01/10/2018

Hemoconcentrator Registration Guideline.

血液浓缩器注册技术审查指导原则.pdf

This guideline can apply to hemoconcentrator that made of hollow fiber and used during extracorporeal circulation. The blood is enriched by filtration. And the product is provided  in a sterile, non-thermal condition. Only one time use.

01/10/2018

Proton Carbon Ion Therapy System Clinical Evaluation Technical Review Guideline.

质子碳离子治疗系统临床评价技术审查指导原则.pdf

This guideline can apply to proton or carbon ion therapy system. It belongs to medical high-energy ray equipment in the ‘Medical Device Classification Catalog(Year 2002 Version)’  and the MD code is 6832. Also other similar particle beam therapy system shall refer to the related content in this guideline.

1/8/2018

AnimalSource Medical Devices Registration Guideline

动物源性医疗器械注册技术审查指导原则.pdf

This guideline can apply to ABORhD blood type antigen detection card(Column agglutination method) and column agglutination method blood type detection card including ABORhD blood type antigen detection usage.

01/05/2018

Moveable Medical Devices Registration Guideline.

移动医疗器械注册技术审查指导原则.pdf

This guideline can apply to moveable medical devices regisration application. It includes class II and class III medical device products.  

12/29/2017

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