Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - ASA s.r.l

Address:

Via Galileo Galilei 23

ARCUGNANO (VI)

36057

Italy

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

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

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Musculoskeletal/physical therapy laser professional Musculoskeletal/physical therapy laser professional Class IIb

Musculoskeletal/physical therapy laser home-use Musculoskeletal/physical therapy laser home-use Class IIb

Deep-tissue electromagnetic stimulation system home-use Deep-tissue electromagnetic stimulation system home-use Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Musculoskeletal/physical therapy laser professional	Musculoskeletal/physical therapy laser professional	Class IIb
Musculoskeletal/physical therapy laser home-use	Musculoskeletal/physical therapy laser home-use	Class IIb
Deep-tissue electromagnetic stimulation system home-use	Deep-tissue electromagnetic stimulation system home-use	Class IIa