General specimen collection kit - UK MHRA Medical Device Registration

General specimen collection kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 175146. The device is manufactured by KOLPLAST CI SA from Brazil, 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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General specimen collection kit

MHRA Device ID: 175146•Ref: 175146

Device Type

General Medical Device

Devices

General specimen collection kit

Type

Class I

Date Registered

Oct 4, 2024

Last Updated

Jul 5, 2024

Manufacturer Information

Name

KOLPLAST CI SA

Address

Est. Municipal Benedito de Souza, 418

Itupeva, São Paulo, Brazil

Created Date

Jun 30, 2023

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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General specimen collection kit - UK MHRA Medical Device Registration

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Last Updated

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