Pulmonary function analysis system, adult - UK MHRA Medical Device Registration
Pulmonary function analysis system, adult is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 177901. The device is manufactured by PulmOne Advanced Medical Devices, Ltd. from Israel, classified as General Medical Device. The authorized representative in the UK is Medes Ltd..
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Device Type
General Medical Device
Devices
Pulmonary function analysis system, adult
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
May 27, 2024
Address
14 HaMelacha Street
Ra'ananna, Israel
Created Date
Aug 23, 2023
Name
Medes Ltd.Relationship Type
Address
5 Beaumont Gate, Shenley Hil
Radlett, Herts, England, United Kingdom
Postcode: WD77AR
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