Circulating-fluid endometrial-ablation catheter - UK MHRA Medical Device Registration

Circulating-fluid endometrial-ablation catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88940. The device is manufactured by LiNA Medical ApS from Denmark, classified as General Medical Device. The authorized representative in the UK is Compliance Solutions (Lifesciences) 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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Circulating-fluid endometrial-ablation catheter

MHRA Device ID: 88940•Ref: 88940

Device Type

General Medical Device

Devices

Circulating-fluid endometrial-ablation catheter

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Mar 12, 2024

Manufacturer Information

Name

LiNA Medical ApS

Address

Formervangen 5

Glostrup, Denmark

Created Date

Jun 7, 2021

Authorized Representative

Name

Compliance Solutions (Lifesciences) Ltd

Relationship Type

UK Responsible Person

Address

Suite 10, Dunswood House 1 Dunswood Road Cumbernauld

Glasgow, United Kingdom

Postcode: G67 3EN

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Circulating-fluid endometrial-ablation catheter - UK MHRA Medical Device Registration

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