Lumbar spine orthosis - UK MHRA Medical Device Registration

Lumbar spine orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 142391. The device is manufactured by Shijiazhuang AOFEITE IMP & EXP 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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MHRA Registered

General Medical Device

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Lumbar spine orthosis

MHRA Device ID: 142391•Ref: 142391

Device Type

General Medical Device

Devices

Lumbar spine orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 8, 2023

Manufacturer Information

Name

Shijiazhuang AOFEITE IMP & EXP Co., Ltd

Address

No. 202 Plant 4th Layer In Gree Supporting Industrial Park, No. 389 Hengshan Street High-tech District, Shijiazhuang City

Hebei Province, China

Created Date

Mar 29, 2022

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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Other Products from Shijiazhuang AOFEITE IMP & EXP Co., Ltd (6)

Other Products from Same Authorized Representative (10)

Lumbar spine orthosis - 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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