Suture removal kit - UK MHRA Medical Device Registration

Suture removal kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 120439. The device is manufactured by Mediplast AB from Sweden, classified as General Medical Device. The authorized representative in the UK is Qserve Group 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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Suture removal kit

MHRA Device ID: 120439•Ref: 120439

Device Type

General Medical Device

Devices

Suture removal kit

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Mediplast AB

Address

Bronsåldersgatan 2

Malmö, Sweden

Created Date

Dec 13, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Suture removal kit - UK MHRA Medical Device Registration

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