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 - Mediflex Surgical Products

Address:

250 Gibbs Rd

Islandia

NY 11749

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

Externally-anchored laparoscopic retractor Externally-anchored laparoscopic retractor Class I

Surgical instrument assist arm system manually-adjusted Surgical instrument assist arm system manually-adjusted Class I

Surgical retraction system reusable Surgical retraction system reusable Conformity Assessment Certificate Expired 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
Externally-anchored laparoscopic retractor	Externally-anchored laparoscopic retractor	Class I
Surgical instrument assist arm system manually-adjusted	Surgical instrument assist arm system manually-adjusted	Class I
Surgical retraction system reusable	Surgical retraction system reusable Conformity Assessment Certificate Expired	Class IIa