Endotracheal tube cuff inflator - UK MHRA Medical Device Registration

Endotracheal tube cuff inflator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 191795. The device is manufactured by Spengler SAS from France, classified as General Medical Device. The authorized representative in the UK is Compliance Solutions (Lifesciences) 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.

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Endotracheal tube cuff inflator

MHRA Device ID: 191795•Ref: 191795

Device Type

General Medical Device

Devices

Endotracheal tube cuff inflator

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 24, 2024

Manufacturer Information

Name

Spengler SAS

Address

30, rue de Jean Guiramand

Aix-en-Provence, France

Created Date

Apr 20, 2024

Authorized Representative

Name

Compliance Solutions (Lifesciences) Ltd

Relationship Type

UK Responsible Person

Address

Suite 10, Dunswood House 1 Dunswood Road Cumbernauld

Glasgow, United Kingdom

Postcode: G67 3EN

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Endotracheal tube cuff inflator - UK MHRA Medical Device Registration

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