Diagnostic spirometer, professional - UK MHRA Medical Device Registration

Diagnostic spirometer, professional is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 101237. The device is manufactured by Pulmonx Corporation from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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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Diagnostic spirometer, professional

MHRA Device ID: 101237•Ref: 101237

Device Type

General Medical Device

Devices

Diagnostic spirometer, professional

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 3, 2024

Manufacturer Information

Name

Pulmonx Corporation

Address

700 Chesapeake Dr.

Redwood City, CA, United States

Created Date

May 6, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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Diagnostic spirometer, professional - UK MHRA Medical Device Registration

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