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 - EPflex Feinwerktechnik GmbH

Address:

Im Schwöllbogen 24

Dettingen an der Erms

72581

Germany

Authorised Representative/ UK Responsible Person
Name: MEDAGENT INTERNATIONAL UK LIMITED
Address:

2 St Andrews Place

Lewes

East Sussex BN7 1UP

England United Kingdom

Code/Term Type

Cardiac/peripheral vascular guidewire single-use Cardiac/peripheral vascular guidewire single-use Class III

Stone/foreign-body extraction set Stone/foreign-body extraction set Class IIa

Stone/foreign-body extraction set Stone/foreign-body extraction set 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
Cardiac/peripheral vascular guidewire single-use	Cardiac/peripheral vascular guidewire single-use	Class III
Stone/foreign-body extraction set	Stone/foreign-body extraction set	Class IIa
Stone/foreign-body extraction set	Stone/foreign-body extraction set	Class I