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NGPOD GLOBAL LIMITED

United Kingdom (ex Northern Ireland) GB-MF-000012817 Last updated 23 May 2026

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Devices
24
Registries
EUDAMED
FDA recalls
0

Catalogue24

Authorised representatives

What NGPOD GLOBAL LIMITED makes

NGPOD Global Limited manufactures reusable, modular sensor devices designed for monitoring physiological parameters in clinical and research settings. These sensors are intended for repeated use and are configured for integration with digital health platforms to collect real-time data.

The company’s sensor portfolio is classified as Class I medical devices under EU regulations and is registered in the EUDAMED database. The devices are 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 NGPOD Global Limited manufacture?

NGPOD Global Limited specializes in reusable, modular sensor devices. These sensors are designed to monitor physiological parameters in clinical and research environments. They are built to be integrated with digital health platforms, enabling real-time data collection for tracking patient or subject metrics.

Where is NGPOD Global Limited based?

NGPOD Global Limited is headquartered in the United Kingdom. This location is relevant for regulatory purposes, as it indicates the primary jurisdiction for the company’s medical devices under EU regulations.

Which regulatory registries list NGPOD Global Limited’s devices?

NGPOD Global Limited’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This registry tracks devices authorized for placement on the EU market, ensuring transparency and compliance with EU medical device regulations.

How are NGPOD Global Limited’s devices classified under EU regulations?

NGPOD Global Limited’s sensor devices fall under Class I classification in the EU. This classification is determined based on factors like the risk associated with the device’s intended use and its design. Class I devices are generally considered low-risk, but they still require compliance with EU Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR) where applicable.

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

Information

Country
United Kingdom (ex Northern Ireland)
Address
UNIT 7, BERKLEY COURT, RUNCORN, United Kingdom (ex Northern Ireland)
Phone
+44 (0) 1616966400
PRRC contact
Clare Unsworth
EUDAMED SRN
GB-MF-000012817