Abdominal aorta endovascular stent-graft - UK MHRA Medical Device Registration

Abdominal aorta endovascular stent-graft is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 79020. The device is manufactured by Lifetech Scientific (Shenzhen) Co Ltd from China, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) 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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MHRA Registered

General Medical Device

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Abdominal aorta endovascular stent-graft

MHRA Device ID: 79020

Device Type

General Medical Device

Devices

Abdominal aorta endovascular stent-graft

Type

Class III

Date Registered

Apr 28, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Name

Lifetech Scientific (Shenzhen) Co Ltd

Address

8F, LifeTech Scientific Building, No.22, Keji 12th Road South, High-tech Industrial Park, Yuehai Subdistrict,

Shenzhen, Nanshan District, China

Created Date

Apr 28, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

DJ Fang

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Other Products from Lifetech Scientific (Shenzhen) Co Ltd (10)

Other Products from Same Authorized Representative (10)

Abdominal aorta endovascular stent-graft - 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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Abdominal aorta endovascular stent-graft

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