What do I have to do to verify the packaging for CE marking of medical devices?

TOPMEN joint announcement body SNCH for domestic enterprises to provide comprehensive medical device product certification services, with a view to enterprises to meet the European Union CE requirements, while we will make full use of our internationalized platform, to provide more comprehensive services for medical device enterprises. We use different certification modes to provide certification services for manufacturers of different medical device products. Our services include:

1.Product classification determination

2.Technical documentation assistance for enterprises

3.Management assistance for enterprises

4.Testing of products

5.Factory audits (where applicable)

6. Certificate Issuance

Background

1. UK-based global multinational corporation; with offices in 56 countries around the world and more than 30,000 registered customers of all types;

2. Asia-Pacific headquartered in Shanghai, providing customers with fast, professional and trustworthy services;

3. Technical experts who have been involved in the research and development of European regulations for a long time. Our technical experts have been involved in the research and development of European regulations for a long time, and have decades of experience in product and system certification, providing customers with one-stop solutions;

4. Our certified products cover a wide range of different categories of medical devices, and the number of certified customers is more than 300;

5. Our open and fair certification process ensures that our customers can monitor our services throughout the whole process. Testing and AuditingCurrently, we have localized our testing and auditing, i.e., all testing and auditing will be conducted domestically by domestic staff, which can save the cost and testing cycle of enterprises.

Auqida Medical Device Consulting Organization