Pulmonary resuscitator, manual, single-use - UK MHRA Medical Device Registration
Pulmonary resuscitator, manual, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 175120. The device is manufactured by Mercury Medical from United States, classified as General Medical Device. The authorized representative in the UK is Advena 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
Pulmonary resuscitator, manual, single-use
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Jul 11, 2024
Name
Mercury MedicalAddress
11300 49th Street North Florida
Clearwater, United States
Created Date
Aug 10, 2021
Name
Advena LtdRelationship Type
Address
Pure Offices Plato Close
Warwick, England, United Kingdom
Postcode: CV34 6WE
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