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

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Manufacturer's Devices - Axis Medicare Ltd

Address:

UNIT 1 VANGUARD INDUSTRIAL ESTATE HENWOOD

ASHFORD

KENT TN24 8DH

United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Human chorionic gonadotropin beta-core fragment IVD kit rapid ICT clinical Human chorionic gonadotropin beta-core fragment IVD kit rapid ICT clinical IVD Devices for Self-Testing

Luteinizing hormone (LH) IVD kit rapid ICT clinical Luteinizing hormone (LH) IVD kit rapid ICT clinical IVD Devices for Self-Testing

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
Human chorionic gonadotropin beta-core fragment IVD kit rapid ICT clinical	Human chorionic gonadotropin beta-core fragment IVD kit rapid ICT clinical	IVD Devices for Self-Testing
Luteinizing hormone (LH) IVD kit rapid ICT clinical	Luteinizing hormone (LH) IVD kit rapid ICT clinical	IVD Devices for Self-Testing