Lumbar decompression procedure kit - UK MHRA Medical Device Registration

Lumbar decompression procedure kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 138496. The device is manufactured by joimax GmbH from Germany, 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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Lumbar decompression procedure kit

MHRA Device ID: 138496•Ref: 138496

Device Type

General Medical Device

Devices

Lumbar decompression procedure kit

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

joimax GmbH

Address

Amalienbadstr. 41 RaumFabrik 61

Karlsruhe, Baden Württemberg, Germany

Created Date

Apr 23, 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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Lumbar decompression procedure kit - UK MHRA Medical Device Registration

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