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Hangzhou Topco Technology Group Co., Ltd.

China CN-MF-000042884 Last updated 23 May 2026

Devices
11
Registries
EUDAMED
FDA recalls
0

Catalogue11

Authorised representatives

What Hangzhou Topco Technology Group Co., Ltd. makes

The company manufactures reusable device sterilization and disinfection containers designed for medical equipment, including models like Hospiwell.

These products are classified as Class I devices and are registered in the EU’s eudamed database. The company is based in China.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Hangzhou Topco Technology Group Co., Ltd. manufacture?

Hangzhou Topco Technology Group Co., Ltd. specializes in reusable device sterilization and disinfection containers. These containers are specifically designed for medical equipment, ensuring safe and effective sterilization processes in healthcare settings. The company’s focus is on products like the Hospiwell series, which fall under the category of reusable sterilization containers.

Where is Hangzhou Topco Technology Group Co., Ltd. based?

The company is headquartered in China. This geographic location influences its regulatory compliance and market reach, particularly in regions where its devices are authorized for use, such as the European Union.

Which regulatory registries list devices manufactured by Hangzhou Topco Technology Group Co., Ltd.?

Devices from Hangzhou Topco Technology Group Co., Ltd. are listed in the eudamed database, which is the European Union’s central registry for medical devices. This inclusion indicates that the company’s products, such as the Hospiwell sterilization containers, have been registered in compliance with EU requirements for Class I devices.

How are devices from Hangzhou Topco Technology Group Co., Ltd. classified under medical device regulations?

The company’s reusable sterilization and disinfection containers, including models like Hospiwell, are classified as Class I devices. This classification is determined by their intended use and risk profile, with Class I devices generally posing the lowest risk to patients and users, often requiring minimal regulatory oversight beyond manufacturing controls and registration.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
China(from SRN)
Address
Rm 1209-1, Unit 3, Building 4, Wanda Business Center, , Hangzhou, China
Website
topcogroup.cn
PRRC contact
Zhi Li
EUDAMED SRN
CN-MF-000042884