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 - Schiller Medical

Address:

4 Rue Louis Pasteur

Wissembourg

67160

France

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

Physiologic-monitoring defibrillation system Physiologic-monitoring defibrillation system Class IIb

Non-rechargeable public automated external defibrillator Non-rechargeable public automated external defibrillator Class IIb

MRI-patient physiologic monitoring system MRI-patient physiologic monitoring system Class IIb

Multiple vital physiological parameter monitoring system clinical Multiple vital physiological parameter monitoring system clinical Class IIb

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
Physiologic-monitoring defibrillation system	Physiologic-monitoring defibrillation system	Class IIb
Non-rechargeable public automated external defibrillator	Non-rechargeable public automated external defibrillator	Class IIb
MRI-patient physiologic monitoring system	MRI-patient physiologic monitoring system	Class IIb
Multiple vital physiological parameter monitoring system clinical	Multiple vital physiological parameter monitoring system clinical	Class IIb