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 - KingSystems

Address:

15011 Herriman Boulevard

Noblesville

IN 46060

United States

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

First Floor Incubator 2 Alconbury Weald Enterprise Campus

Alconbury Weald

Huntingdon

Cambridgeshire PE28 4XA

United Kingdom

Code/Term Type

Laryngoscope blade single-use Laryngoscope blade single-use Class I

Microbial medical gas filter single-use Microbial medical gas filter single-use Class IIa

Rigid laryngopharyngoscope Rigid laryngopharyngoscope 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
Laryngoscope blade single-use	Laryngoscope blade single-use	Class I
Microbial medical gas filter single-use	Microbial medical gas filter single-use	Class IIa
Rigid laryngopharyngoscope	Rigid laryngopharyngoscope	Class I