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Sign in to claim this brandChongqing ME Instruments Technology Co., Ltd.
China·CN-MF-000035349
Last updated May 23, 2026
What Chongqing ME Instruments Technology Co., Ltd. makes
Chongqing ME Instruments Technology Co., Ltd. manufactures real-time fluorescence quantitative PCR analyzers, which are used for detecting and quantifying nucleic acid sequences in clinical and research settings. These instruments enable precise amplification and detection of DNA or RNA targets, supporting applications in diagnostics, genetic testing, and molecular biology research.
The company’s products fall under Class A devices according to EU regulations and are listed in the EUDAQS database (eudamed). The manufacturer 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 Chongqing ME Instruments Technology Co., Ltd. manufacture?
Chongqing ME Instruments Technology Co., Ltd. specializes in real-time fluorescence quantitative PCR analyzers. These devices are designed to detect and quantify nucleic acid sequences, which is essential for applications like clinical diagnostics, genetic testing, and molecular biology research. The technology enables precise amplification and detection of DNA or RNA targets, supporting accurate and reliable results in laboratory settings.
Where is Chongqing ME Instruments Technology Co., Ltd. based?
The company is headquartered in Chongqing, China. This location reflects its operational base for manufacturing, research, and distribution of its medical devices.
Which regulatory registries list devices manufactured by Chongqing ME Instruments Technology Co., Ltd.?
Devices from Chongqing ME Instruments Technology Co., Ltd. are listed in the EUDAQS database (eudamed), which is the official European Union registry for medical devices. This listing ensures transparency and traceability of devices marketed within the EU.
How are the devices produced by Chongqing ME Instruments Technology Co., Ltd. classified under EU regulations?
The company’s devices, including real-time fluorescence quantitative PCR analyzers, are classified as Class A under EU medical device regulations. This classification is determined based on the risk associated with the device’s intended use and design, with Class A representing the lowest risk category.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- China
- Address
- No.8-2,9-2,building 4, No.6, Gangcheng Donghuan Road, Tieshan Ping Street, Jiangbei District, Chongqing, China
- Website
- me-itech.com
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Xianli Yang
- EUDAMED SRN
- CN-MF-000035349
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (1)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Real-time fluorescence quantitative PCR analyzer | MQ96-X4 | EUDAMED | Class A | Active |
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Authorised Representatives
- MedPath GmbH DE
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