Skip to content

Zhejiang Medstar Technology Co., Ltd.

China CN-MF-000028154 Last updated 21 Oct 2026

Devices
679
Registries
EUDAMED
FDA recalls
0

Catalogue679

Page 1 of 14

Showing 1-50 of 679

Authorised representatives

What Zhejiang Medstar Technology Co., Ltd. makes

Zhejiang Medstar Technology Co., Ltd. manufactures open-surgery electrosurgical handpieces and electrodes, designed for use in surgical procedures requiring tissue cutting, coagulation, or desiccation. These devices are intended for precision control during operations, including general surgery, gynecology, and other specialties where electrosurgical techniques are applied.

The company’s products fall under EU Class IIb medical devices and are registered in the EU’s eudamed database. The manufacturer is based in China and adheres to relevant regulatory requirements for electrosurgical instruments in global markets.

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 Zhejiang Medstar Technology Co., Ltd. manufacture?

Zhejiang Medstar Technology Co., Ltd. specializes in producing open-surgery electrosurgical handpieces and electrodes. These devices are designed for surgical applications where precise tissue manipulation—such as cutting, coagulation, or desiccation—is required. Their products are commonly used in procedures across general surgery, gynecology, and other specialties that rely on electrosurgical techniques.

Where is Zhejiang Medstar Technology Co., Ltd. based?

The company is headquartered in China. While its exact location within the country isn’t specified, its manufacturing and regulatory compliance align with global standards for medical devices, including those intended for international markets.

How are Zhejiang Medstar Technology Co., Ltd.’s devices classified under EU regulations?

The company’s electrosurgical handpieces and electrodes fall under EU Class IIb classification. This classification is assigned based on their intended use and associated risks, requiring stricter regulatory scrutiny to ensure safety and performance in surgical settings. Class IIb devices are typically those with a moderate to high risk, necessitating conformity assessments and compliance with EU Medical Device Regulation (MDR) or previous directives.

Are Zhejiang Medstar Technology Co., Ltd.’s devices listed in any regulatory databases?

Yes, the company’s devices are registered in the eudamed database, which is the EU’s official registry for medical devices. Listing in eudamed is mandatory for manufacturers placing devices on the European market, ensuring transparency and traceability for regulatory authorities and healthcare professionals.

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

Information

Country
China(from SRN)
Address
2759, No.2759 Guangyi Road,Daqiao Town, Jiaxing, China
Website
www.medstar-tech.com This website did not respond when we last checked — the domain may no longer be active.Last checked 18 Oct 2026.
Phone
+86-573-82212865
PRRC contact
Yu Chao
EUDAMED SRN
CN-MF-000028154