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Pulmonary function analysis system, adult - UK MHRA Medical Device Registration

Pulmonary function analysis system, adult is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 183418. The device is manufactured by Restech S.R.L. from Italy, classified as General Medical Device. The authorized representative in the UK is Donawa Lifescience 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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Pulmonary function analysis system, adult
MHRA Device ID: 183418โ€ขRef: 183418

Device Type

General Medical Device

Devices

Pulmonary function analysis system, adult

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 7, 2023

Manufacturer Information

Address

via Melchiorre Gioia, 63

Milan, Italy

Created Date

Apr 20, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

Aviation Business Park Enterprise Close

Christchurch, England, United Kingdom

Postcode: BH23 6NX

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