Fentanyl IVD, reagent - UK MHRA Medical Device Registration

Fentanyl IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178053. The device is manufactured by Assure Tech. (Hangzhou) Co., Ltd., from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap 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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Fentanyl IVD, reagent

MHRA Device ID: 178053•Ref: 178053

Device Type

In Vitro Diagnostic Device

Devices

Fentanyl IVD, reagent

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Mar 23, 2024

Manufacturer Information

Name

Assure Tech. (Hangzhou) Co., Ltd.,

Address

Building 4, No 1418-50 Moganshan Road Gongshu District

Zheijiang, Hangzhou, China

Created Date

May 12, 2022

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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Other Products from Assure Tech. (Hangzhou) Co., Ltd., (10)

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Fentanyl IVD, reagent - 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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