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 - Blue Leaves Paper Production LLC

Address:

WH18C and 18D

Umm Deraa

Umm Al Quwain DIP 2

United Arab Emirates

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

Northside House Mount Pleasant

Barnet

EN4 9EE

United Kingdom

Code/Term Type

Absorbent underpad non-antimicrobial single-use Absorbent underpad non-antimicrobial 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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