Shenzhen Class III Medical Device License Application

2025年二类医疗器械备案

Require

，根据医疗器械监督管理条例凡是从事二类医疗器械经营的单位都需要到所在地设区的市级食品药品监督管理部门备案，二类医疗器械是具有中度风险，需要控制管理以保证其安全、effective medical device。

like：医用缝合针、sphygmomanometer、thermometer、心电图机、脑电图机、microscope、acupuncture needle、生化分析系统、hearing aid、超声消毒设备、不可吸收缝合线等。下面小编为大家解答，Shenzhen Class III Medical Device License Application：经营A类产品的企业经营场所使用面积应不小于100平方米.仓库使用面积应不小于20平方米。

经营B类产品的企业经营场所使用面积应不小于60平方米、仓库使用面积应不小于20平方米。经营C类产品的企业经营场所使用面积应不小于50平方米、仓库使用面积应不小于60平方米。经营D类产品的企业.经营场所使用面积含同一址仓库应不低于60平方米。

经营E类产品的企业.经营场所使用面积含同一址仓库应不小于60平方米。经营F类产品的企业经营场所使用面积应不小于40平方米、仓库使用面积应不小于20平方米。

Our company has currently assisted thousands of medical device companies to register and sell，Good reputation from customers，As we all know, the reason why customers of medical device sales companies look for agents is simply because they don’t have a warehouse.，No registered address，and personnel。

Because you only open one，So you don't have much experience，And we are specialized in this industry，So we know every step inside.，If you want to open a medical device sales company, you can consult our company at any time.，You are more welcome to come to our company for negotiation，The purpose of our company is：Shenzhen Class III Medical Device License Application，a cooperation，lifelong friend。The content of this article is strictly prohibited from being reproduced by any website or individual.，Violators will be prosecuted。

Related products：Medical device transfer , Medical device registration , Apply for medical devices

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