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 - Bistos Co. Ltd.

Address:

7th Fl. A Bldg Woolim Lions Valley 5-cha 302

Galmachi-ro Jungwon-gu

Seongnam-si

Gyeonggi-do 13201

South Korea

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Overhead infant phototherapy unit Overhead infant phototherapy unit Class IIa

Breast pump electric Breast pump electric Class IIa

Foetal cardiac monitor Foetal cardiac monitor

Foetal Doppler system Foetal Doppler system

Pulse oximeter Pulse oximeter Class IIb

Head-worn lamp Head-worn lamp Class I

Breast pump support kit reusable Breast pump support kit reusable 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
Overhead infant phototherapy unit	Overhead infant phototherapy unit	Class IIa
Breast pump electric	Breast pump electric	Class IIa
Foetal cardiac monitor	Foetal cardiac monitor
Foetal Doppler system	Foetal Doppler system
Pulse oximeter	Pulse oximeter	Class IIb
Head-worn lamp	Head-worn lamp	Class I
Breast pump support kit reusable	Breast pump support kit reusable	Class I