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Wendy0519
We are a Non-EU medical device manufacturer which has CE and ISO 13485 certificate. Doctors from UK and Belgium hospital would to use our product ( category IIb) now, but we don’t have any distributors in the Europe.
I would like to know,
1) Could we sale our product from China to EU hospitals directly?
2) If so, is there any specific requirements for hospitals?
I would like to know,
1) Could we sale our product from China to EU hospitals directly?
2) If so, is there any specific requirements for hospitals?