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 - LifeGlobal Group LLC

Address:

393 Soundview Road

Guilford

Connecticut 03467

United States

Authorised Representative/ UK Responsible Person
Name: Research Instruments Limited
Address:

Bickland Industrial Park

Falmouth

Cornwall TR11 4TA

United Kingdom

Code/Term Type

Medical gas pipeline system air filter Medical gas pipeline system air filter Class I

IVF medium kit IVF medium kit Class III

Assisted reproduction procedure dish Assisted reproduction procedure dish Class IIa

IVF medium IVF medium Class III

Non-respiratory device ambient air filter Non-respiratory device ambient air filter Class IIa

Non-respiratory device ambient air filter Non-respiratory device ambient air filter Class I

Non-respiratory device ambient air filter Non-respiratory device ambient air filter Class I

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
Medical gas pipeline system air filter	Medical gas pipeline system air filter	Class I
IVF medium kit	IVF medium kit	Class III
Assisted reproduction procedure dish	Assisted reproduction procedure dish	Class IIa
IVF medium	IVF medium	Class III
Non-respiratory device ambient air filter	Non-respiratory device ambient air filter	Class IIa
Non-respiratory device ambient air filter	Non-respiratory device ambient air filter	Class I
Non-respiratory device ambient air filter	Non-respiratory device ambient air filter	Class I