Manual goniometer - UK MHRA Medical Device Registration

Manual goniometer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 181005. The device is manufactured by Meloq AB from Sweden, classified as General Medical Device. The authorized representative in the UK is Wellkang 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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Manual goniometer

MHRA Device ID: 181005•Ref: 181005

Device Type

General Medical Device

Devices

Manual goniometer

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 8, 2024

Manufacturer Information

Name

Meloq AB

Address

Drakenbergsgatan 3

Stockholm, Sweden

Created Date

Oct 30, 2023

Authorized Representative

Name

Wellkang Ltd

Relationship Type

UK Responsible Person

Address

16 Castle St.

Dover, Kent, England, United Kingdom

Postcode: CT16 1PW

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Other Products from Meloq AB (1)

Back/leg/chest dynamometer, electronic

Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Manual goniometer - UK MHRA Medical Device Registration

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