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 - Vygon (UK) Ltd

Address:

The Pierre Simonet Building V Park Gateway North Latham Road

Swindon

Wiltshire SN25 4DL

United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Vascular catheter introduction set nonimplantable Vascular catheter introduction set nonimplantable

Arterial/central venous catheterization support/maintenance kit non-medicated Arterial/central venous catheterization support/maintenance kit non-medicated

Epidural/intrathecal anaesthesia set non-medicated Epidural/intrathecal anaesthesia set non-medicated

Peripherally-inserted central venous catheter Peripherally-inserted central venous catheter

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
Vascular catheter introduction set nonimplantable	Vascular catheter introduction set nonimplantable
Arterial/central venous catheterization support/maintenance kit non-medicated	Arterial/central venous catheterization support/maintenance kit non-medicated
Epidural/intrathecal anaesthesia set non-medicated	Epidural/intrathecal anaesthesia set non-medicated
Peripherally-inserted central venous catheter	Peripherally-inserted central venous catheter