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 - AST Products Inc.

Address:

9 Linnell Circle

Billerica MA

01821

United States

Authorised Representative/ UK Responsible Person
Name: MDSS-UK RP LIMITED
Address:

6 Wilmslow Road Rusholme

Manchester

M14 5TP

England United Kingdom

Code/Term Type

Intraocular lens-insertion cartridge Intraocular lens-insertion cartridge Class IIa

Posterior-chamber intraocular lens pseudophakic Posterior-chamber intraocular lens pseudophakic Class IIb

Manual intraocular lens injector single-use Manual intraocular lens injector single-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
Intraocular lens-insertion cartridge	Intraocular lens-insertion cartridge	Class IIa
Posterior-chamber intraocular lens pseudophakic	Posterior-chamber intraocular lens pseudophakic	Class IIb
Manual intraocular lens injector single-use	Manual intraocular lens injector single-use	Class IIa