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 - EmergoPharm Spóka z ograniczona odpowiedzialnoci Sp. K.

Address:

Józefa Pisudskiego 11

Konstancin-Jeziorna

05-510

Poland

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Ear dropper reusable Ear dropper reusable Class III

Nasal mucosa dressing non-antimicrobial Nasal mucosa dressing non-antimicrobial 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
Ear dropper reusable	Ear dropper reusable	Class III
Nasal mucosa dressing non-antimicrobial	Nasal mucosa dressing non-antimicrobial	Class I