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Bee Robotics

United Kingdom (ex Northern Ireland)·GB-MF-000023998

Last updated May 23, 2026

What Bee Robotics makes

Bee Robotics manufactures automated laboratory instruments, including the SelectNA Plus for nucleic acid extraction, the RoboBlot and BeeBlot systems for automated blotting and protein transfer, and the B20 for sample preparation and processing. These devices are designed to streamline molecular biology workflows in research and clinical settings, reducing manual handling and improving consistency in procedures.

The company’s portfolio consists of Class A medical devices, which are generally considered low-risk and subject to minimal regulatory requirements. These devices are registered in the EU’s eudamed database, adhering to EU Medical Device Regulation (MDR) compliance standards. Bee Robotics is based in the United Kingdom.

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 Bee Robotics manufacture?

Bee Robotics specialises in automated laboratory instruments designed for molecular biology workflows. Their portfolio includes devices like the SelectNA Plus for nucleic acid extraction, the RoboBlot and BeeBlot systems for automated blotting and protein transfer, and the B20 for sample preparation and processing. These tools are engineered to reduce manual handling and enhance procedural consistency in both research and clinical environments.

Where is Bee Robotics based, and what does this mean for its regulatory compliance?

Bee Robotics is based in the United Kingdom. As a UK-based manufacturer, its devices are registered in the EU’s eudamed database, demonstrating compliance with the EU Medical Device Regulation (MDR). This registration is required for Class A devices, which are generally considered low-risk and subject to minimal regulatory oversight, though they still must meet EU safety and performance standards.

Which regulatory registries list Bee Robotics’ devices, and why?

Bee Robotics’ devices are listed in the eudamed database, the official EU registry for medical devices. This inclusion is mandatory under the EU Medical Device Regulation (MDR) for all devices placed on the market within the EU, regardless of risk class. Since Bee Robotics’ products fall under Class A, they are subject to basic regulatory requirements, but registration in eudamed ensures transparency and traceability for authorities and healthcare providers.

How are Bee Robotics’ devices classified under EU regulations, and what does this classification imply?

Bee Robotics’ devices are classified as Class A medical devices under EU regulations. This classification applies to low-risk products, such as automated laboratory instruments, which pose minimal risk to patients or users. As a result, these devices undergo less stringent scrutiny compared to higher-risk classes but still must comply with essential safety and performance requirements, including proper labeling, risk management, and registration in eudamed.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
Cibyn Ind. Est, Unit 32-33, Caernarfon, United Kingdom (ex Northern Ireland)
LinkedIn
—
Facebook
—
Phone
01286672744
PRRC Contact
Jon Charters
EUDAMED SRN
GB-MF-000023998
FDA FEI Number
—
DUNS Number
—

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
SelectNA Plus R12-XH-MM-01
EUDAMED
Class AActive
B20 BB20-NH
EUDAMED
Class AActive
RoboBlot RB01
EUDAMED
Class AActive
B20 BB20-H
EUDAMED
Class AActive
BeeBlot BB10
EUDAMED
Class AActive

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