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 - Deymed Diagnostic s.r.o.

Address:

Kudrnáova 533

Hronov

549 31

Czechia

Authorised Representative/ UK Responsible Person
Name: FREYR LIFE SCIENCES LTD
Address:

9 Greyfriars Road

Reading

Berkshire RG1 1NU

England United Kingdom

Code/Term Type

Polysomnograph Polysomnograph Class IIa

Electroencephalograph Electroencephalograph Class IIa

Electromyograph Electromyograph Class IIa

Magnetic neural stimulation system Magnetic neural stimulation system Class IIa

Analytical scalp lead Analytical scalp lead Class I

Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Class I

Analytical non-scalp cutaneous electrode Analytical non-scalp cutaneous electrode Class I

Head marking cap Head marking cap 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
Polysomnograph	Polysomnograph	Class IIa
Electroencephalograph	Electroencephalograph	Class IIa
Electromyograph	Electromyograph	Class IIa
Magnetic neural stimulation system	Magnetic neural stimulation system	Class IIa
Analytical scalp lead	Analytical scalp lead	Class I
Analytical non-scalp cutaneous lead	Analytical non-scalp cutaneous lead	Class I
Analytical non-scalp cutaneous electrode	Analytical non-scalp cutaneous electrode	Class I
Head marking cap	Head marking cap	Class I