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 - Delcath Systems Inc

Address:

566 Queensbury Ave Queensbury

New York

12804

United States

Authorised Representative/ UK Responsible Person
Name: Regulis Consulting Limited
Address:

Wessex House Marlow Road

Bourne End

Buckinghamshire SL8 5SP

England United Kingdom

Code/Term Type

Haemoperfusion system Haemoperfusion system Class IIb

Haemoperfusion system Haemoperfusion system Class III

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
Haemoperfusion system	Haemoperfusion system	Class IIb
Haemoperfusion system	Haemoperfusion system	Class III