Needle guide, single-use - UK MHRA Medical Device Registration

Needle guide, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 212658. The device is manufactured by DIXI Medical from France, classified as General Medical Device.

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MHRA Registered

General Medical Device

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Needle guide, single-use

MHRA Device ID: 212658

Device Type

General Medical Device

Type

Class III

Status

DREGIY

Date Registered

Mar 10, 2025

Manufacturer Information

Name

DIXI Medical

Address

2A route de Pouligney Chaudefontaine

Marchaux-Chaudefontaine, France

DJ Fang

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Needle guide, single-use - UK MHRA Medical Device Registration

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