Carbon dioxide cuvette, single-use - UK MHRA Medical Device Registration
Carbon dioxide cuvette, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 184323. The device is manufactured by AirLife Finland Oy from Finland, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting 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
Carbon dioxide cuvette, single-use
Type
Class IIa
Date Registered
Sep 24, 2024
Last Updated
Mar 26, 2024
Relationship Type
Address
Beaver House, 23-38 Hythe Bridge Street
Oxford, England, United Kingdom
Postcode: OX1 2EP
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