Reinforced endotracheal tube, single-use - UK MHRA Medical Device Registration

Reinforced endotracheal tube, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 197288. The device is manufactured by Venner Medical (Singapore) Pte Ltd. from Singapore, 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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Reinforced endotracheal tube, single-use

MHRA Device ID: 197288•Ref: 197288

Device Type

General Medical Device

Devices

Reinforced endotracheal tube, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jun 7, 2024

Manufacturer Information

Name

Venner Medical (Singapore) Pte Ltd.

Address

35 Joo Koon Circle

Singapore, Singapore

Created Date

Jul 2, 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 Venner Medical (Singapore) Pte Ltd. (10)

Other Products from Same Authorized Representative (10)

Reinforced endotracheal tube, 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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