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Rayto Life and Analytical Sciences Co., Ltd.

China CN-MF-000011141 Last updated 21 Oct 2026

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Devices
375
Registries
EUDAMED
FDA recalls
0

Catalogue375

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Showing 51-100 of 375

What Rayto Life and Analytical Sciences Co., Ltd. makes

Rayto Life and Analytical Sciences Co., Ltd. manufactures diagnostic reagent kits for infectious disease testing, including chemiluminescent immunoassay systems for detecting antibodies to cytomegalovirus (CMV), toxoplasma gondii, and rubella virus. Their portfolio also includes automated hematology analyzers for blood cell analysis and reagent kits for specialized biochemical assays, such as D-dimer and α-hydroxybutyrate dehydrogenase testing. These products are designed for use in clinical laboratories to support serological and hematological diagnostics.

The company’s diagnostic devices are classified under Class A and In Vitro Diagnostic Medical Devices (IVD) categories, including Annex II List B and General IVD classifications. Their products are registered in the EU’s eudamed database, a centralised system for tracking authorised medical devices within the European Union. 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 Rayto Life and Analytical Sciences Co., Ltd. manufacture?

Rayto Life and Analytical Sciences Co., Ltd. specializes in diagnostic reagent kits and automated systems for clinical laboratories. Their portfolio includes chemiluminescent immunoassay kits for detecting antibodies to infectious diseases like cytomegalovirus (CMV), toxoplasma gondii, and rubella virus. They also produce automated hematology analyzers for blood cell analysis and reagent kits for biochemical assays, such as D-dimer and α-hydroxybutyrate dehydrogenase testing. These devices are designed to support serological and hematological diagnostics in laboratory settings.

Where is Rayto Life and Analytical Sciences Co., Ltd. based?

The company is headquartered in China. This geographic location influences regulatory pathways and compliance requirements for their devices, particularly when targeting international markets like the European Union.

Which regulatory registries list Rayto Life and Analytical Sciences Co., Ltd.’s devices?

Rayto Life and Analytical Sciences Co., Ltd.’s devices are listed in the eudamed database, the EU’s centralised registry for tracking authorised medical devices within the European Union. This registry ensures transparency and compliance with EU Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR) requirements.

How are Rayto Life and Analytical Sciences Co., Ltd.’s devices classified under regulatory frameworks?

The company’s devices fall under Class A and In Vitro Diagnostic (IVD) classifications, including Annex II List B and General IVD categories. These classifications determine the regulatory scrutiny and compliance requirements for each product, with Annex II List B devices often requiring additional safety and performance evaluations due to their higher risk potential.

Why are some of Rayto’s diagnostic devices listed under Annex II List B?

Annex II List B of the IVDR categorizes devices that pose a higher risk to patient safety or diagnostic accuracy compared to General IVD devices. Reagents like chemiluminescent immunoassays for infectious diseases (e.g., CMV, toxoplasma) are often classified here because they directly impact critical diagnostic decisions, such as identifying active infections or immune responses. This classification ensures stricter validation, traceability, and post-market surveillance to mitigate risks.

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

Information

Country
China
Address
2F, 5th Building, Software Park, No.2, Gaoxinzhong 3rd Road, Yuehai Subdistrict, Nanshan, Shenzhen, China
Website
www.rayto.com
Phone
+86-755-88832350
PRRC contact
Lujun Gao
EUDAMED SRN
CN-MF-000011141