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 - Harol S.r.l.

Address:

Via Marcora 53

San Donato Milanese

Milano 20097

Italy

Authorised Representative/ UK Responsible Person
Name: MDQ Services Ltd
Address:

Flat 81 Seacon Tower 5 Hutching’s Street

London

England E14 8JX

England United Kingdom

Code/Term Type

PEEP valve single-use PEEP valve single-use Class IIa

Oxygen administration hood adult Oxygen administration hood adult Class IIa

Oxygen administration hood paediatric Oxygen administration hood paediatric Class IIa

CPAP/BPAP face mask single-use CPAP/BPAP face mask 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
PEEP valve single-use	PEEP valve single-use	Class IIa
Oxygen administration hood adult	Oxygen administration hood adult	Class IIa
Oxygen administration hood paediatric	Oxygen administration hood paediatric	Class IIa
CPAP/BPAP face mask single-use	CPAP/BPAP face mask single-use	Class IIa