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 - Heraeus Medical Components LLC

Address:

5030 Centerville Road

St. Paul

Minnesota 55127

United States

Authorised Representative/ UK Responsible Person
Name: MPS Medical-Product-Service UK Ltd
Address:

Northgate House Northgate Street

Devizes

Wiltshire SN10 1JX

England United Kingdom

Code/Term Type

Vena cava filter extraction/repositioning kit Vena cava filter extraction/repositioning kit Class III

Gastro-urological guidewire single-use Gastro-urological guidewire single-use 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
Vena cava filter extraction/repositioning kit	Vena cava filter extraction/repositioning kit	Class III
Gastro-urological guidewire single-use	Gastro-urological guidewire single-use	Class IIa