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 - Worldwide Innovations & Technologies Inc.

Address:

14740 W. 101st Terrace

Lenexa

KS 66215

United States

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

Livingstone House 309 Harrow Road

Wembley

Middlesex HA9 6BD

England United Kingdom

Code/Term Type

Patient radiation shielding pad/drape reusable Patient radiation shielding pad/drape reusable Class I

Patient radiation shielding pad/drape single-use Patient radiation shielding pad/drape 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

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Code/Term		Type
Patient radiation shielding pad/drape reusable	Patient radiation shielding pad/drape reusable	Class I
Patient radiation shielding pad/drape single-use	Patient radiation shielding pad/drape single-use	Class I