Dry powder inhaler - UK MHRA Medical Device Registration

Dry powder inhaler is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 132282. The device is manufactured by Laboratorios Liconsa, S.A. from Spain, classified as General Medical Device. The authorized representative in the UK is Asphalion Limited.

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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Dry powder inhaler

MHRA Device ID: 132282•Ref: 132282

Device Type

General Medical Device

Devices

Dry powder inhaler

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 20, 2024

Manufacturer Information

Name

Laboratorios Liconsa, S.A.

Address

Calle Dulcinea, S/N

Alcalá de Henares, Madrid, Spain

Created Date

Jan 13, 2022

Authorized Representative

Name

Asphalion Limited

Relationship Type

UK Responsible Person

Address

19 The Circle, Queen Elizabeth Street

London, England, United Kingdom

Postcode: SE1 2JE

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Dry powder inhaler - UK MHRA Medical Device Registration

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