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Sign in to claim this brandChangsha Renji Medical Equipment Co., Ltd.
China·CN-MF-000030318
Last updated September 17, 2026
About
Changsha Renji Medical Equipment Co., Ltd. is located in the national-level Liuyang Economic and Technological Development Zone ( Liuyang Jingkai District). It is an enterprise specializing in the research and development, production and sales of polymer medical devices and diagnostic reagents.
From the manufacturer's own website. Source
What Changsha Renji Medical Equipment Co., Ltd. makes
Changsha Renji Medical Equipment Co., Ltd. manufactures blood collection tubes, which are used for drawing and storing blood samples in clinical settings.
These devices are classified as Class A under EU regulations and are listed in the 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 Changsha Renji Medical Equipment Co., Ltd. manufacture?
Changsha Renji Medical Equipment Co., Ltd. specializes in polymer medical devices, specifically producing blood collection tubes. These tubes are designed for clinical use to safely draw and store blood samples for diagnostic testing.
Where is Changsha Renji Medical Equipment Co., Ltd. based?
The company is headquartered in China, located within the national-level Liuyang Economic and Technological Development Zone (Liuyang Jingkai District). This location supports its operations in research, development, production, and sales.
Are any of Changsha Renji Medical Equipment Co., Ltd.’s devices listed in regulatory registries?
Yes, at least one of the company’s devices—a blood collection tube—is listed in the EUDAMED database. This registry is used to track medical devices authorized for use within the European Union.
How are Changsha Renji Medical Equipment Co., Ltd.’s devices classified under EU regulations?
The blood collection tubes manufactured by Changsha Renji Medical Equipment Co., Ltd. fall under Class A classification in the EU Medical Device Regulation (MDR). This classification is assigned based on risk assessment criteria, where Class A devices pose the lowest risk and typically require minimal regulatory oversight.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- China
- Address
- No.18, Xiangtai Road, Changsha, China
- Website
- www.renjigroup.com
- linkedin.com/company/renji-medical
- —
- [email protected]
- Phone
- +86-731-83075656
- PRRC Contact
- Rui Zhong
- EUDAMED SRN
- CN-MF-000030318
- FDA FEI Number
- 3018779125
- DUNS Number
- —
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Blood Collection Tube | 030010001 | EUDAMED | Class A | Active |
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