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 205232. The device is manufactured by Henan Tuoren Medical Device Co., Ltd from China, classified as General Medical Device. The authorized representative in the UK is SUNGO Certification Company 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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Pulmonary resuscitator, manual, single-use

MHRA Device ID: 205232•Ref: 205232

Device Type

General Medical Device

Devices

Pulmonary resuscitator, manual, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 25, 2024

Manufacturer Information

Name

Henan Tuoren Medical Device Co., Ltd

Address

Weiyuan Industrial Zone, Menggang, Changyuan County

Henan Province, China

Created Date

May 23, 2022

Authorized Representative

Name

SUNGO Certification Company Limited

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

DJ Fang

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Other Products from Henan Tuoren Medical Device Co., Ltd (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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