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 - SIE Surgical Instrument Engineering

Address:

Allmendstrasse 11

Port

2562

Switzerland

Authorised Representative/ UK Responsible Person
Name: Instinctive Limited
Address:

Instinctive Ltd 201 Silbury Boulevard

Milton Keynes

Buckinghamshire MK9 1LZ

England United Kingdom

Code/Term Type

Femtosecond ophthalmic solid-state laser system Femtosecond ophthalmic solid-state laser system Class IIb

Ophthalmic surgical procedure kit non-medicated single-use Ophthalmic surgical procedure kit non-medicated single-use

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
Femtosecond ophthalmic solid-state laser system	Femtosecond ophthalmic solid-state laser system	Class IIb
Ophthalmic surgical procedure kit non-medicated single-use	Ophthalmic surgical procedure kit non-medicated single-use