Pulmonary resuscitator, manual, single-use - UK MHRA Medical Device Registration

Pulmonary resuscitator, manual, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 175120. The device is manufactured by Mercury Medical from United States, classified as General Medical Device. The authorized representative in the UK is Advena 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 resuscitator, manual, single-use

MHRA Device ID: 175120•Ref: 175120

Device Type

General Medical Device

Devices

Pulmonary resuscitator, manual, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jul 11, 2024

Manufacturer Information

Name

Mercury Medical

Address

11300 49th Street North Florida

Clearwater, United States

Created Date

Aug 10, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

DJ Fang

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Other Products from Mercury Medical (10)

Other Products from Same Authorized Representative (10)

Pulmonary resuscitator, manual, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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