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 - Heinz Meise GmbH Medizintechnik

Address:

Im Gewerbepark 6

Schalksmühle

58579

Germany

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

Eye dropper bottle Eye dropper bottle Class IIa

Inspiratory/expiratory limb respiratory tubing single-use Inspiratory/expiratory limb respiratory tubing single-use Class IIa

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
Eye dropper bottle	Eye dropper bottle	Class IIa
Inspiratory/expiratory limb respiratory tubing single-use	Inspiratory/expiratory limb respiratory tubing single-use	Class IIa