Pulse oximeter probe, single-use - UK MHRA Medical Device Registration
Pulse oximeter probe, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 106692. The device is manufactured by Philips Medical Systems (Andover) from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics 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
Pulse oximeter probe, single-use
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Aug 31, 2024
Address
3000 Minuteman Road
Andover, United States
Created Date
Oct 4, 2021
Relationship Type
Address
Ascent 1 Farnborough Aerospace Centre
Farnborough, Hampshire, England, United Kingdom
Postcode: GU14 6XW
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