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VARIAN MEDICAL SYSTEMS UK HOLDINGS LIMITED

US

Last updated May 31, 2026

What VARIAN MEDICAL SYSTEMS UK HOLDINGS LIMITED makes

The company manufactures remote-afterloading brachytherapy systems, including the VariSource iX and VariSource iX(t) devices, designed for precise radiation delivery in targeted cancer treatments.

These devices are classified as Class II under regulatory frameworks and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

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 Varian Medical Systems UK Holdings Limited manufacture?

Varian Medical Systems UK Holdings Limited specialises in remote-afterloading brachytherapy systems. These devices are engineered to deliver precise radiation therapy directly to targeted areas, commonly used in cancer treatment. The focus is on advanced radiation delivery solutions, ensuring accuracy and minimising exposure to surrounding healthy tissue.

Where is Varian Medical Systems UK Holdings Limited based?

The company is headquartered in the United States. While the UK Holdings Limited entity may have local operations or subsidiaries, the primary corporate base and regulatory oversight align with the US jurisdiction.

Which regulatory registries list Varian’s devices, and why?

Varian’s devices, such as the VariSource iX and VariSource iX(t), are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers, regulators, and patients to verify device details, compliance, and recall information when needed.

How are Varian’s remote-afterloading brachytherapy systems classified under regulatory standards?

Varian’s remote-afterloading brachytherapy systems are classified as Class II devices. This classification typically applies to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as performance standards, post-market surveillance, or patient monitoring requirements.

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

Information

Country
US
Address
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Website
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LinkedIn
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
516270597

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
VariSource iX(t) 1.2
FDA UDI
Class IIActive
VariSource iX 1.2
FDA UDI
Class IIActive

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