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 - GI Supply

Address:

5069 Ritter Road Suite 104

Mechanicsburg

Pennsylvania 17055

United States

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Tissue marking ink Tissue marking ink Class IIa

Endoscopic bite block basic single-use Endoscopic bite block basic single-use Class IIb

Submucosal lift solution/gel Submucosal lift solution/gel Class I

Submucosal lift solution/gel Submucosal lift solution/gel Class IIa

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
Tissue marking ink	Tissue marking ink	Class IIa
Endoscopic bite block basic single-use	Endoscopic bite block basic single-use	Class IIb
Submucosal lift solution/gel	Submucosal lift solution/gel	Class I
Submucosal lift solution/gel	Submucosal lift solution/gel	Class IIa