Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

CTF MEG International Services Limited Partnership

US

Last updated May 30, 2026

What CTF MEG International Services Limited Partnership makes

CTF MEG International Services Limited Partnership manufactures superconducting magnetoencephalography (MEG) systems, designed for non-invasive brain imaging to measure and map neural activity through magnetic fields.

The company’s portfolio is regulated under Class II medical devices in the US and is listed in the FDA’s Unique Device Identifier (UDI) database.

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 CTF MEG International Services Limited Partnership primarily manufacture?

CTF MEG International Services Limited Partnership specializes in superconducting magnetoencephalography (MEG) systems. These devices are designed for non-invasive brain imaging, allowing researchers and clinicians to measure and map neural activity by detecting magnetic fields generated by brain function. The focus is on advanced neuroimaging technology for scientific and clinical applications.

Where is CTF MEG International Services Limited Partnership based?

The company is based in the United States. While the exact location isn’t specified, its regulatory filings and device listings confirm its operational presence within the US market.

Which regulatory registries or databases list CTF MEG’s devices?

CTF MEG’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class II medical devices, including the company’s superconducting MEG systems, which fall under this classification in the US.

How are CTF MEG’s devices classified under US regulations?

The company’s superconducting magnetoencephalography systems are classified as Class II medical devices in the US. This classification typically applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.

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

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
203364765

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Ctf Meg CTF MEG 275
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.