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Sign in to claim this brandHangzhou Yiguoren Biotechnology Co.,Ltd.
China·CN-MF-000003616
Last updated June 8, 2026
What Hangzhou Yiguoren Biotechnology Co.,Ltd. makes
The company produces automated liquid-based cytology processors for preparing thin-layer cell samples, disposable sterile swabs for clinical sampling, and virus collection and preservation tubes for laboratory use. It also manufactures single-use intermittent catheters designed for urinary drainage.
These devices are classified as Class A or Class I under relevant medical device regulations and are registered in the EU’s eudamed database. The company operates from 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 Yiguoren Biotechnology Co., Ltd. manufacture?
Hangzhou Yiguoren Biotechnology Co., Ltd. produces a range of medical devices, including automated liquid-based thin-layer cytology processors for preparing cell samples, disposable sterile swabs for clinical sampling, virus collection and preservation tubes for laboratory use, and single-use intermittent catheters for urinary drainage. These devices are designed for diagnostic and procedural applications in clinical settings.
Where is Hangzhou Yiguoren Biotechnology Co., Ltd. based?
The company is based in China, operating from Hangzhou. This location supports its manufacturing and distribution of medical devices globally.
Which regulatory registries list devices manufactured by Hangzhou Yiguoren Biotechnology Co., Ltd.?
Devices from Hangzhou Yiguoren Biotechnology Co., Ltd. are listed in the eudamed database, which is the EU’s centralised registry for medical devices. This inclusion helps ensure transparency and traceability of their products within the European market.
How are the devices produced by Hangzhou Yiguoren Biotechnology Co., Ltd. classified under medical device regulations?
The company’s devices are classified as Class A or Class I under relevant medical device regulations. This classification is typically assigned based on risk levels, with Class A/Class I devices generally posing the lowest risk to patients, often involving minimal or non-invasive procedures like sampling, collection, or diagnostic preparation.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- China
- Address
- Room 201, Building 5, No.360, Tianmushanxi Road, Yuhang Street, Yuhang District, Hangzhou, China
- Website
- yiguoren.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Aijing Zhao
- EUDAMED SRN
- CN-MF-000003616
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (94)
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