Wart-removal material - UK MHRA Medical Device Registration

Wart-removal material is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 120217. The device is manufactured by PK Benelux BV from Netherlands, 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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Wart-removal material

MHRA Device ID: 120217•Ref: 120217

Device Type

General Medical Device

Devices

Wart-removal material

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

PK Benelux BV

Address

Vluchtoord 17

Uden, Noord Brabant, Netherlands

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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Other Products from PK Benelux BV (7)

Other Products from Same Authorized Representative (10)

Wart-removal material - 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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