Medical Device AIMDD Active Implant Instruction , China Medical Device AIMDD Active Implant Instruction Supplier

Medical Device AIMDD Active Implant Instruction - a1

Medical Device AIMDD Active Implant Instruction For Sale, Most Competitive Price, Fast Delivery, Custom Service, Wholesale Medical Device AIMDD Active Implant Instruction , Made in China, High Quality Products!, China AIMDD, Consulting Supplier, Manufacturer.

AIMDD instruction was drawn up in 1990 and was applied for compulsory matters since January, 1995. Therefore, selling active implant medical device in Europe must paste CE tags. Manufacturers must prove to the certification authorities that products which paste CE tags meet the AIMDD instructions:
Type testing
Designing evaluation
Medical device evaluation for producers (ISO13485/ ISO9001)
Clinical report evaluation
Meet the requirements on all the medical devices instructions.
Osmunda, a consulting organization engaged in medical devices regulations consulting, medical devices registration agent, medical device managerial system certification and medical device products certification, focuses on providing international medical device registration, medical device system certification for medical device enterprises. Besides, osmunda can help medical device suppliers with audition of the second and third party and examine goods for export, providing information of manufacturing license consulting service.

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Osmunda Medical Device Consulting CO.LTD

Address: 7th Floor,JinGui business center,CongYun road No.982,Baiyun, Guangzhou, Guangdong, China,
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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.