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Foetal Doppler system probe - UK MHRA Medical Device Registration

Foetal Doppler system probe is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 115219. The device is manufactured by ArjoHuntleigh AB from Sweden, classified as General Medical Device. The authorized representative in the UK is Arjo UK Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Foetal Doppler system probe
MHRA Device ID: 115219

Device Type

General Medical Device

Devices

Foetal Doppler system probe

Type

Class I

Date Registered

Feb 16, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Address

Hans Michelsensgaten 10

Malmo, Sweden

Created Date

Feb 16, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

ArjoHuntleigh House Houghton Hall Business Park

Houghton Regis, Bedfordshire, England, United Kingdom

Postcode: LU5 5XF

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