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 - Meridian Medical d.o.o

Address:

Ljubljana Plemljeva ulica 8

1210 Ljubljana

Sentvid

EU

Slovenia

Authorised Representative/ UK Responsible Person
Name: HAAG STREIT UK LTD
Address:

Unit A Cartel Business Estate

EDINBURGH WAY

HARLOW

ESSEX CM20 2TT

United Kingdom

Code/Term Type

Ophthalmic solid-state laser system photodisruption Ophthalmic solid-state laser system photodisruption Class IIb

Ophthalmic solid-state laser system Ophthalmic solid-state laser system Class IIb

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
Ophthalmic solid-state laser system photodisruption	Ophthalmic solid-state laser system photodisruption	Class IIb
Ophthalmic solid-state laser system	Ophthalmic solid-state laser system	Class IIb