Diagnostic spirometer, professional - UK MHRA Medical Device Registration
Diagnostic spirometer, professional is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 101237. The device is manufactured by Pulmonx Corporation from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP LIMITED.
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
Diagnostic spirometer, professional
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Apr 3, 2024
Address
700 Chesapeake Dr.
Redwood City, CA, United States
Created Date
May 6, 2021
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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