Keratolytic solution - UK MHRA Medical Device Registration

Keratolytic solution is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 205588. The device is manufactured by Biocool AB from Sweden, classified as General Medical Device. The authorized representative in the UK is Adveniunt Medical International Limited (trading as Quality First International).

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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Keratolytic solution

MHRA Device ID: 205588•Ref: 205588

Device Type

General Medical Device

Devices

Keratolytic solution

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 23, 2024

Manufacturer Information

Name

Biocool AB

Address

Malmskillnadsgatan 39

Stockholm, Sweden

Created Date

Nov 21, 2024

Authorized Representative

Name

Adveniunt Medical International Limited (trading as Quality First International)

Relationship Type

UK Responsible Person

Address

1 Cooks Road Stratford

London, England, United Kingdom

Postcode: E15 2PW

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Other Products from Biocool AB (1)

Corn/callus softening agent

Type: General Medical Device

Registered: Nov 26, 2024

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Keratolytic solution - UK MHRA Medical Device Registration

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