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 - bess pro gmbh

Address:

Gustav-Krone-Straße 7

Berlin

14167

Germany

Authorised Representative/ UK Responsible Person
Name: Advena Ltd
Address:

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Polymer-metal tracheal/bronchial stent Polymer-metal tracheal/bronchial stent Class IIb

Polymer-metal oesophageal stent Polymer-metal oesophageal stent Class IIb

Silicone-sheet tissue reconstructive material sterile Silicone-sheet tissue reconstructive material sterile Class IIa

Tracheobronchial guidewire Tracheobronchial guidewire Class IIb

Tracheobronchial guidewire Tracheobronchial guidewire 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
Polymer-metal tracheal/bronchial stent	Polymer-metal tracheal/bronchial stent	Class IIb
Polymer-metal oesophageal stent	Polymer-metal oesophageal stent	Class IIb
Silicone-sheet tissue reconstructive material sterile	Silicone-sheet tissue reconstructive material sterile	Class IIa
Tracheobronchial guidewire	Tracheobronchial guidewire	Class IIb
Tracheobronchial guidewire	Tracheobronchial guidewire	Class IIa