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 - SteriPack USA Limited

Address:

4255 South Pipkin Road

Lakeland

Florida 33811

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

Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Class I

General-purpose absorbent tip applicator/swab single-use General-purpose absorbent tip applicator/swab single-use 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
Oral/upper respiratory tract specimen collection swab	Oral/upper respiratory tract specimen collection swab	Class I
General-purpose absorbent tip applicator/swab single-use	General-purpose absorbent tip applicator/swab single-use	Class I