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 177901. The device is manufactured by PulmOne Advanced Medical Devices, Ltd. from Israel, classified as General Medical Device. The authorized representative in the UK is Medes Ltd..

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Pulmonary function analysis system, adult

MHRA Device ID: 177901•Ref: 177901

Device Type

General Medical Device

Devices

Pulmonary function analysis system, adult

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

May 27, 2024

Manufacturer Information

Name

PulmOne Advanced Medical Devices, Ltd.

Address

14 HaMelacha Street

Ra'ananna, Israel

Created Date

Aug 23, 2023

Authorized Representative

Name

Medes Ltd.

Relationship Type

UK Responsible Person

Address

5 Beaumont Gate, Shenley Hil

Radlett, Herts, England, United Kingdom

Postcode: WD77AR

DJ Fang

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Type: General Medical Device

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

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