Electrocardiographic recording paper - UK MHRA Medical Device Registration

Electrocardiographic recording paper is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 184322. The device is manufactured by AirLife Finland Oy from Finland, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting 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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Electrocardiographic recording paper

MHRA Device ID: 184322•Ref: 184322

Device Type

General Medical Device

Devices

Electrocardiographic recording paper

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 12, 2024

Manufacturer Information

Name

AirLife Finland Oy

Address

Kuortaneenkatu 2

Helsinki, Finland

Created Date

Jan 9, 2024

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

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Electrocardiographic recording paper - UK MHRA Medical Device Registration

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