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 - ELESTA S.p.A.

Address:

Via Baldanzese 17

Calenzano

Firenze 50041

Italy

Authorised Representative/ UK Responsible Person
Name: Lynton Lasers Ltd
Address:

Unit 9D Holmes Chapel Business Centre

Manor Lane

Holmes Chapel

Cheshire CW48AF

England United Kingdom

Code/Term Type

General/multiple surgical laser system beam guide single-use General/multiple surgical laser system beam guide single-use Class IIa

Body aspiration needle single-use Body aspiration needle single-use Class IIa

Ultrasound-guided laser thermal therapy needle guide positioning system Ultrasound-guided laser thermal therapy needle guide positioning system Class I

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
General/multiple surgical laser system beam guide single-use	General/multiple surgical laser system beam guide single-use	Class IIa
Body aspiration needle single-use	Body aspiration needle single-use	Class IIa
Ultrasound-guided laser thermal therapy needle guide positioning system	Ultrasound-guided laser thermal therapy needle guide positioning system	Class I