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 - Redsense Medical AB

Address:

Box 7088

Halmstad

300 07

Sweden

Authorised Representative/ UK Responsible Person
Name: Health Tec Medical Limited
Address:

Unit 11 Hathersage Park

Heather Lane Hathersage

Hope Valley

Derbyshire S32 1DP

England United Kingdom

Code/Term Type

Intravenous access site line-disconnection monitoring system Intravenous access site line-disconnection monitoring system Class I

Intravenous access site monitoring system fibreoptic cable reusable Intravenous access site monitoring system fibreoptic cable reusable Class I

Intravenous access site monitoring system fibreoptic cable single-use Intravenous access site monitoring system fibreoptic cable 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
Intravenous access site line-disconnection monitoring system	Intravenous access site line-disconnection monitoring system	Class I
Intravenous access site monitoring system fibreoptic cable reusable	Intravenous access site monitoring system fibreoptic cable reusable	Class I
Intravenous access site monitoring system fibreoptic cable single-use	Intravenous access site monitoring system fibreoptic cable single-use	Class I