Exhaled-gas oesophageal intubation detector, adult - UK MHRA Medical Device Registration
Exhaled-gas oesophageal intubation detector, adult is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 102597. The device is manufactured by Engineered Medical Systems, Inc dba Pulmodyne from United States, classified as General Medical Device. The authorized representative in the UK is QNET 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
Exhaled-gas oesophageal intubation detector, adult
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Nov 7, 2023
Address
2055 Executive Drive
Indianapolis, Indianapolis, United States
Created Date
Sep 3, 2021
Name
QNET LtdRelationship Type
Address
Livingstone House 309 Harrow Road
Wembley, Middlesex, England, United Kingdom
Postcode: HA9 6BD
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