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 197913. 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.
Device Type
General Medical Device
Devices
Foetal Doppler system probe
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Jul 2, 2024
Name
Arjo UK LtdRelationship Type
Address
ArjoHuntleigh House Houghton Hall Business Park
Houghton Regis, Bedfordshire, England, United Kingdom
Postcode: LU5 5XF
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