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TIANJIN KANGLI MEDICAL APPLIANCE CO., LTD

China·CN-MF-000035399

Last updated May 23, 2026

What TIANJIN KANGLI MEDICAL APPLIANCE CO., LTD makes

The company manufactures the Kang Jun, a medical device designed for use in surgical procedures, specifically as a surgical instrument or retractor. These devices are intended to assist in maintaining exposure and access during operations, ensuring optimal working conditions for surgeons.

The Kang Jun falls under Class I medical devices in the European Union, as listed in the EUDAMED registry. The company is based in China and adheres to relevant regulatory standards for Class I devices in its market.

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 Tianjin Kangli Medical Appliance Co., Ltd manufacture?

Tianjin Kangli Medical Appliance Co., Ltd manufactures the Kang Jun, a surgical instrument or retractor. These devices are specifically designed to assist surgeons by maintaining exposure and access during surgical procedures, helping to create optimal working conditions.

Where is Tianjin Kangli Medical Appliance Co., Ltd based?

The company is headquartered in China. This location places it within the regulatory framework of the Chinese medical device market, though its devices may also be listed in international registries like EUDAMED.

Which regulatory registries list Tianjin Kangli Medical Appliance Co., Ltd’s devices?

The company’s devices, including the Kang Jun, are listed in the EUDAMED registry. This registry is used to track medical devices placed on the European market, ensuring transparency and traceability for Class I devices.

How are Tianjin Kangli Medical Appliance Co., Ltd’s devices classified in the European Union?

The Kang Jun devices fall under Class I classification in the European Union. This classification is determined by their intended use as surgical retractors, which are considered low-risk devices under EU regulations. Class I devices typically require fewer regulatory controls but must still comply with essential safety and performance requirements.

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

Information

Country
China
Address
NO.5, SHENGYUAN ROAD,FUYUAN ECONOMIC REGION,MEICHANG TOWN, WUQING DISTRICT,, TIANJIN , China
Website
tjkangli.com
LinkedIn
—
Facebook
—
Phone
—
PRRC Contact
Andy Wang
EUDAMED SRN
CN-MF-000035399
FDA FEI Number
—
DUNS Number
—

Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Kang Jun V-01
EUDAMED
Class IActive
Kang Jun A-17
EUDAMED
Class IActive
Kang Jun B-1
EUDAMED
Class IActive
Kang Jun F-W01
EUDAMED
Class IActive

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