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 - ENDO-FLEX GmbH

Address:

Alte Hünxer Straße 115

Voerde

46562

Germany

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

ERCP catheter non-balloon non-electrical single-use ERCP catheter non-balloon non-electrical single-use Class I

Endoscopic stent-placement system Endoscopic stent-placement system Class I

Polymeric biliary stent non-bioabsorbable Polymeric biliary stent non-bioabsorbable Class IIb

Endoscopic electrosurgical handpiece/electrode monopolar single-use Endoscopic electrosurgical handpiece/electrode monopolar single-use Class IIb

Body aspiration needle single-use Body aspiration needle 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
ERCP catheter non-balloon non-electrical single-use	ERCP catheter non-balloon non-electrical single-use	Class I
Endoscopic stent-placement system	Endoscopic stent-placement system	Class I
Polymeric biliary stent non-bioabsorbable	Polymeric biliary stent non-bioabsorbable	Class IIb
Endoscopic electrosurgical handpiece/electrode monopolar single-use	Endoscopic electrosurgical handpiece/electrode monopolar single-use	Class IIb
Body aspiration needle single-use	Body aspiration needle single-use	Class IIa