News & Events

2017-09-04 New Medical Device Classification Catalog
2017-09-04 Surgical Astral Lamp Registration Guideline
2017-09-01 Medical Device Classification Determination
2017-08-31 Imported Medical Devices CFDA Registered Items Alteration Guideline
2017-08-29 Dental Planter CFDA Registration Unit Division
2017-08-28 Dental Planter CFDA Registration Guideline
2017-08-24 Medical Nebulizer CFDA Registration Inspection Concerns
2017-08-23 Active Medical Devices CFDA Registration Units Partition
2017-08-22 How to Compile Contraindications, Notices, Warning and Tips in the Medical Device Manual for the CFDA Registration
2017-08-21 Medical Device Manual Requirements for the CFDA Registration
2017-08-18 How to Compile Clinical Evaluation for Medical Nebulizer CFDA Registration
2017-08-17 Medical Nebulizer Registration Guideline
2017-08-16 Free Webinar! CFDA New Notification about Standardize the Use of Chinese Name for Foreign Medical Device CFDA Registration
2017-08-15 Pre-market Regulatory Analysis
2017-08-15 Pre-market Regulatory Analysis
2017-08-14 Registration Guidelines for the Medical Electronic Thermometers
2017-08-11 CFDA to Implement Registration Technical Guidelines for Medical Device Network Security
2017-08-10 Four Important Measures to Promote the Reform of Medical Device Registration Management in 2017
2017-08-09 Foreign Medical Device Applicant are Required to Supplement the Chinese Information to CFDA
2017-08-08 China Legal Agents of Medical Device
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CIRS China

Ms. Shuo Wang (Head office)
Tel: +86-571 8720 6559 | Fax: +86-571 87206533
Mr. Edwin Wen (Beijing office)
Tel: +86-10 63984062 | Fax: +86-10 63984032

CIRS Europe

Ms. Louise Halpin
Tel: +353 41 9806 916 | Fax: +353 41 9806 999