Aerosol face mask, rebreathing, single-use - UK MHRA Medical Device Registration
Aerosol face mask, rebreathing, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 209871. The device is manufactured by Medline Industries, LP from United States, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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
Type
Class IIa
Status
Date Registered
Jan 31, 2025
Address
Three Lakes Drive
Northfield, United States
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