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 - Seer medical Pty Ltd

Address:

278 Queensberry Street

Melbourne

3000

Australia

Authorised Representative/ UK Responsible Person
Name: Seer Medical UK Pty Ltd
Address:

Studio G10.1 Battersea Studio 1

80 Silverthorne Rd

London

SW8 3HE

England United Kingdom

Code/Term Type

Electroencephalographic ambulatory recorder Electroencephalographic ambulatory recorder Class IIa

Electrocardiography telemetric monitoring system Electrocardiography telemetric monitoring system 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
Electroencephalographic ambulatory recorder	Electroencephalographic ambulatory recorder	Class IIa
Electrocardiography telemetric monitoring system	Electrocardiography telemetric monitoring system	Class IIa