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 - Nalge Nunc International Corporation

Address:

75 Panorama Creek Drive Rochester

New York

14625

United States

Authorised Representative/ UK Responsible Person
Name: Life Technologies Ltd
Address:

3 Fountain Drive Inchinnan Business Park

Paisley

Renfrewshire PA4 9RF

United Kingdom

Code/Term Type

General tissue specimen container IVD no additive General tissue specimen container IVD no additive IVD General

General specimen container IVD no additive/medium General specimen container IVD no additive/medium IVD General

Assisted reproduction procedure dish Assisted reproduction procedure dish 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
General tissue specimen container IVD no additive	General tissue specimen container IVD no additive	IVD General
General specimen container IVD no additive/medium	General specimen container IVD no additive/medium	IVD General
Assisted reproduction procedure dish	Assisted reproduction procedure dish	Class IIa