Intravenous administration bag/bottle - UK MHRA Medical Device Registration

Intravenous administration bag/bottle is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95154. The device is manufactured by Jiangsu Kangjin Medical Instrument Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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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Intravenous administration bag/bottle

MHRA Device ID: 95154•Ref: 95154

Device Type

General Medical Device

Devices

Intravenous administration bag/bottle

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jun 26, 2024

Manufacturer Information

Name

Jiangsu Kangjin Medical Instrument Co., Ltd.

Address

Zhenglu Town, Changzhou City

Jiangsu Province, China

Created Date

Aug 16, 2021

Authorized Representative

Name

SUNGO Certification Company Limited

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

DJ Fang

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Intravenous administration bag/bottle - 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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