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 - Top Corporation

Address:

19-10 Senju Nakai-cho Adachi-ku

Tokyo

120-0035

Japan

Authorised Representative/ UK Responsible Person
Name: MPS Medical-Product-Service UK Ltd
Address:

Northgate House Northgate Street

Devizes

Wiltshire SN10 1JX

England United Kingdom

Code/Term Type

Haematological concentrate/haemostatic agent applicator cannula endoscopic single-use Haematological concentrate/haemostatic agent applicator cannula endoscopic single-use Class IIa

Endoscope observation cap single-use Endoscope observation cap single-use Class IIa

Nerve-locating anaesthesia needle Nerve-locating anaesthesia needle Class IIa

Radio-frequency ablation system Radio-frequency ablation system 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
Haematological concentrate/haemostatic agent applicator cannula endoscopic single-use	Haematological concentrate/haemostatic agent applicator cannula endoscopic single-use	Class IIa
Endoscope observation cap single-use	Endoscope observation cap single-use	Class IIa
Nerve-locating anaesthesia needle	Nerve-locating anaesthesia needle	Class IIa
Radio-frequency ablation system	Radio-frequency ablation system	Class IIb