Inspiratory line humidification chamber, single-use - UK MHRA Medical Device Registration

Inspiratory line humidification chamber, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96761. 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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Inspiratory line humidification chamber, single-use

MHRA Device ID: 96761•Ref: 96761

Device Type

General Medical Device

Devices

Inspiratory line humidification chamber, single-use

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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Other Products from DEAS Srl (10)

Other Products from Same Authorized Representative (10)

Inspiratory line humidification chamber, single-use - UK MHRA Medical Device Registration

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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