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 - Vigmed AB

Address:

Kungsgatan 6

SE-252 21 Helsingborg

SE-252 21

Sweden

Authorised Representative/ UK Responsible Person
Name: Greiner Bio-One Limited
Address:

Brunel Way Stroudwater Business Park

Stonehouse

Gloucestershire

GL10 3SX

United Kingdom

Code/Term Type

Peripheral intravenous cannula Peripheral intravenous cannula Class IIa

Peripheral artery cannula Peripheral artery cannula 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
Peripheral intravenous cannula	Peripheral intravenous cannula	Class IIa
Peripheral artery cannula	Peripheral artery cannula	Class IIa