Nasal oxygen cannula, CPAP - UK MHRA Medical Device Registration

Nasal oxygen cannula, CPAP is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96766. The device is manufactured by DEAS Srl from Italy, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, 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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Nasal oxygen cannula, CPAP

MHRA Device ID: 96766•Ref: 96766

Device Type

General Medical Device

Devices

Nasal oxygen cannula, CPAP

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

DEAS Srl

Address

Via dell'Industria 49

Castel Bolognese, RA, Italy

Created Date

Aug 20, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Nasal oxygen cannula, CPAP - UK MHRA Medical Device Registration

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