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 - Toul Meditech AB

Address:

Tunbytorpsgatan 31

Vasteras

SE-721 37

Sweden

Authorised Representative/ UK Responsible Person
Name: Vision Pharmaceuticals Ltd (Spectrum)
Address:

Fernbank House Tytherington Business Park

Springwood Way

Macclesfield

Cheshire SK10 2XA

England United Kingdom

Code/Term Type

Surgical laminar airflow unit Surgical laminar airflow unit Class I

Patient surgical drape single-use Patient surgical 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
Surgical laminar airflow unit	Surgical laminar airflow unit	Class I
Patient surgical drape single-use	Patient surgical drape single-use	Class I