Guidewire-retention prevention box - UK MHRA Medical Device Registration

Guidewire-retention prevention box is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 117508. 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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Guidewire-retention prevention box

MHRA Device ID: 117508•Ref: 117508

Device Type

General Medical Device

Devices

Guidewire-retention prevention box

Type

Class I

Date Registered

Nov 10, 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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Guidewire-retention prevention box - UK MHRA Medical Device Registration

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