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 - Diversatek Healthcare Inc

Address:

9150 Commerce Center Circle Suite 500

Highlands Ranch

Colorado

80129

United States

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Manometric gastrointestinal motility analysis system Manometric gastrointestinal motility analysis system Conformity Assessment Certificate Expired Class IIa

Manometric gastrointestinal motility analysis system Manometric gastrointestinal motility analysis system 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
Manometric gastrointestinal motility analysis system	Manometric gastrointestinal motility analysis system Conformity Assessment Certificate Expired	Class IIa
Manometric gastrointestinal motility analysis system	Manometric gastrointestinal motility analysis system	Class IIa