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 - Aurolab

Address:

1 Sivagangai Main Road Veerapanjan

Madurai

625020

India

Authorised Representative/ UK Responsible Person
Name: Daybreak Medical Ltd
Address:

Unit 4 St Lawrence Business Centre Victoria Road

Feltham

TW13 7LT

England United Kingdom

Code/Term Type

Vitreous/aqueous humour replacement medium intraoperative Vitreous/aqueous humour replacement medium intraoperative 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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