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

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Manufacturer's Devices - Cowellmedi

Address:

48 Hakgam-daero 22lbeon-gil

Busan

Sasang-gu 46986

South Korea

Authorised Representative/ UK Responsible Person
Name: UKCA Experts Ltd.
Address:

Dept 302 43 Owston Road Carcroft

Doncaster

DN6 8DA

England United Kingdom

Code/Term Type

Dental/maxillofacial surgical procedure kit non-medicated reusable Dental/maxillofacial surgical procedure kit non-medicated reusable Class I

Screw endosteal dental implant two-piece Screw endosteal dental implant two-piece Class IIb

Dental implant suprastructure permanent preformed Dental implant suprastructure permanent preformed Class IIb

Pliable-polymer dental regeneration membrane bioabsorbable tacked Pliable-polymer dental regeneration membrane bioabsorbable tacked 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
Dental/maxillofacial surgical procedure kit non-medicated reusable	Dental/maxillofacial surgical procedure kit non-medicated reusable	Class I
Screw endosteal dental implant two-piece	Screw endosteal dental implant two-piece	Class IIb
Dental implant suprastructure permanent preformed	Dental implant suprastructure permanent preformed	Class IIb
Pliable-polymer dental regeneration membrane bioabsorbable tacked	Pliable-polymer dental regeneration membrane bioabsorbable tacked	Class IIa