United Kingdom MHRA device registration 175265

General surgical procedure kit, non-medicated, single-use

United Kingdom·System or Procedure Pack·HEMODIA SAS·Registered Nov 26, 2024

Registration details

Device ID: 175265
MHRA Reference Number: 175265
Date Registered: Nov 26, 2024
Last Updated: Oct 30, 2024

Device classification

Device Type: System or Procedure Pack
Devices: General surgical procedure kit, non-medicated, single-use
Type: System or Procedure Pack

Manufacturer

Name: HEMODIA SAS
Address: 85, rue du Chêne vert
Labège, France
Created Date: Sep 9, 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

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About this record

General surgical procedure kit, non-medicated, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 175265. The device is manufactured by HEMODIA SAS from France, classified as System or Procedure Pack. 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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