Deep-tissue electromagnetic stimulation system, home-use - UK MHRA Medical Device Registration

Deep-tissue electromagnetic stimulation system, home-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195174. The device is manufactured by ASA s.r.l from Italy, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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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Deep-tissue electromagnetic stimulation system, home-use

MHRA Device ID: 195174•Ref: 195174

Device Type

General Medical Device

Devices

Deep-tissue electromagnetic stimulation system, home-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 9, 2024

Manufacturer Information

Name

ASA s.r.l

Address

Via Galileo Galilei, 23

ARCUGNANO (VI), Italy

Created Date

Sep 1, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

DJ Fang

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Other Products from ASA s.r.l (4)

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Deep-tissue electromagnetic stimulation system, home-use - 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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Deep-tissue electromagnetic stimulation system, home-use

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