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 98795. The device is manufactured by Ventlab LLC. from United States, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting 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: 98795•Ref: 98795

Device Type

General Medical Device

Devices

Pulmonary resuscitator, manual, single-use

Type

Class IIa

Date Registered

Apr 11, 2024

Last Updated

Oct 5, 2023

Manufacturer Information

Name

Ventlab LLC.

Address

2710 Northridge Dr. Suite A

Grand Rapids, MI, United States

Created Date

Aug 25, 2021

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

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Other Products from Ventlab LLC. (3)

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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