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

Back to MHRA

Manufacturer's Devices - Ganshorn Medizin Electronic GMBH

Address:

Industrie-Strasse 6-8

Niederlauer

97618

Germany

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

200 Brook Drive Green Park

Reading

Berkshire RG2 6UB

England United Kingdom

Code/Term Type

Diagnostic spirometer professional Diagnostic spirometer professional Class IIa

Whole-body plethysmograph Whole-body plethysmograph Class IIa

Pulmonary function analysis system adult Pulmonary function analysis system adult Class IIa

Cardiopulmonary stress exercise monitoring system Cardiopulmonary stress exercise monitoring system Class IIa

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

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Diagnostic spirometer professional	Diagnostic spirometer professional	Class IIa
Whole-body plethysmograph	Whole-body plethysmograph	Class IIa
Pulmonary function analysis system adult	Pulmonary function analysis system adult	Class IIa
Cardiopulmonary stress exercise monitoring system	Cardiopulmonary stress exercise monitoring system	Class IIa
Benchtop nebulizer non-heated	Benchtop nebulizer non-heated	Class IIa