Test tube/reservoir cap IVD - UK MHRA Medical Device Registration

Test tube/reservoir cap IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 145925. The device is manufactured by Citotest Labware Manufacturing Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Wellkang 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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Test tube/reservoir cap IVD

MHRA Device ID: 145925•Ref: 145925

Device Type

In Vitro Diagnostic Device

Devices

Test tube/reservoir cap IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Nov 15, 2023

Manufacturer Information

Name

Citotest Labware Manufacturing Co., Ltd.

Address

No.339 Beihai West Road,

Haimen City, Jiangsu Province, China

Created Date

Jan 25, 2021

Authorized Representative

Name

Wellkang Ltd

Relationship Type

Authorised Representative (Northern Ireland)

Address

Enterprise Hub, NW Business Complex 1 Beraghmore Road

Derry, Northern Ireland, Northern Ireland, United Kingdom

Postcode: BT48 8SE

DJ Fang

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Other Products from Citotest Labware Manufacturing Co., Ltd. (10)

Other Products from Same Authorized Representative (10)

Test tube/reservoir cap IVD - 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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