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Skin autofluorescence analyser - UK MHRA Medical Device Registration

Skin autofluorescence analyser is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 89097. The device is manufactured by DiagnOptics Technologies B.V. 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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Skin autofluorescence analyser
MHRA Device ID: 89097•Ref: 89097

Device Type

General Medical Device

Devices

Skin autofluorescence analyser

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Address

Aarhusweg 4-9

Groningen, Groningen, Netherlands

Created Date

Jul 15, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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