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

Back to MHRA

Manufacturer's Devices - Sapi Med S.p.A.

Address:

Via della chimica 6 – Z.I. D3

Alessandria

15121

Italy

Authorised Representative/ UK Responsible Person
Name: P3 Medical Ltd
Address:

Unit 1 Newbridge Close

Newbridge Trading Estate

Bristol

BS4 4AX

England United Kingdom

Code/Term Type

Proctoscope single-use Proctoscope single-use Class I

Rectoscope single-use Rectoscope single-use Class I

Haemorrhoid ligator Haemorrhoid ligator Class I

Manual rectal irrigation system Manual rectal irrigation system Class I

Endoscopic light source unit line-powered Endoscopic light source unit line-powered Class I

Fibreoptic light cable Fibreoptic light cable Class I

Fibreoptic light cable Fibreoptic light cable Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Proctoscope single-use	Proctoscope single-use	Class I
Rectoscope single-use	Rectoscope single-use	Class I
Haemorrhoid ligator	Haemorrhoid ligator	Class I
Manual rectal irrigation system	Manual rectal irrigation system	Class I
Endoscopic light source unit line-powered	Endoscopic light source unit line-powered	Class I
Fibreoptic light cable	Fibreoptic light cable	Class I
Fibreoptic light cable	Fibreoptic light cable	Class I