Abdominal hernia truss, single-use - UK MHRA Medical Device Registration

Abdominal hernia truss, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 156081. The device is manufactured by HERDEGEN (SAS) from France, classified as General Medical Device. The authorized representative in the UK is AF PHARMA SERVICE UK LTD.

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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Abdominal hernia truss, single-use

MHRA Device ID: 156081•Ref: 156081

Device Type

General Medical Device

Devices

Abdominal hernia truss, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Aug 3, 2023

Manufacturer Information

Name

HERDEGEN (SAS)

Address

5/7 rue Freyssinet

Chelles, France

Created Date

Sep 13, 2022

Authorized Representative

Name

AF PHARMA SERVICE UK LTD

Relationship Type

UK Responsible Person

Address

Suite 140 Temple Chambers 3-7 Temple Avenue

London, England, United Kingdom

Postcode: EC4Y 0DA

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Other Products from HERDEGEN (SAS) (10)

Other Products from Same Authorized Representative (10)

Abdominal hernia truss, single-use - 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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