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 - PARI Pharma GmbH

Address:

Moosstrasse 3

Starnberg

82319

Germany

Authorised Representative/ UK Responsible Person
Name: PARI Medical Ltd
Address:

8 Oyster Park 109 Chertsey Rd Byfleet

8 Oyster Park 109 Cherstey Rd Byfleet

West Byfleet

Surrey KT14 7AX

England United Kingdom

Code/Term Type

Inhalation therapy saline solution hypertonic Inhalation therapy saline solution hypertonic Class IIa

Benchtop nebulizer non-heated Benchtop nebulizer non-heated Class IIa

Aerosol face mask rebreathing single-use Aerosol face mask rebreathing single-use Class I

Aerosol face mask rebreathing single-use Aerosol face mask rebreathing single-use Class IIa

Aerosol face mask rebreathing single-use Aerosol face mask rebreathing 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
Inhalation therapy saline solution hypertonic	Inhalation therapy saline solution hypertonic	Class IIa
Benchtop nebulizer non-heated	Benchtop nebulizer non-heated	Class IIa
Aerosol face mask rebreathing single-use	Aerosol face mask rebreathing single-use	Class I
Aerosol face mask rebreathing single-use	Aerosol face mask rebreathing single-use	Class IIa
Aerosol face mask rebreathing single-use	Aerosol face mask rebreathing single-use	Class IIa