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 - Axiom Medical Inc

Address:

19320 Van Ness Avenue

Torrance

California 90501

United States

Authorised Representative/ UK Responsible Person
Name: SENSUS Group Ltd
Address:

The Barn Tednambury Farm

Tednambury

Spellbrook

Hertfordshire CM23 4BD

England United Kingdom

Code/Term Type

Closed-wound drain non-bioabsorbable Closed-wound drain non-bioabsorbable Class IIa

Mediastinal drainage catheter non-antimicrobial Mediastinal drainage catheter non-antimicrobial Class IIa

Mediastinal drainage catheter antimicrobial Mediastinal drainage catheter antimicrobial 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
Closed-wound drain non-bioabsorbable	Closed-wound drain non-bioabsorbable	Class IIa
Mediastinal drainage catheter non-antimicrobial	Mediastinal drainage catheter non-antimicrobial	Class IIa
Mediastinal drainage catheter antimicrobial	Mediastinal drainage catheter antimicrobial	Class IIa