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 - Carbon Medical Technologies Inc

Address:

1290 Hammond Road

Saint Paul

Minnesota 55110-5867

United States

Authorised Representative/ UK Responsible Person
Name: Donawa Lifescience Ltd
Address:

Aviation Business Park Enterprise Close

Christchurch

BH23 6NX

England United Kingdom

Code/Term Type

Imaging lesion localization marker implantable Imaging lesion localization marker implantable Class IIb

Submucosal injection needle Submucosal injection needle Class IIb

Urinary tract reconstructive material synthetic polymer non-bioabsorbable Urinary tract reconstructive material synthetic polymer non-bioabsorbable Class IIa

Urinary tract reconstructive material synthetic polymer non-bioabsorbable Urinary tract reconstructive material synthetic polymer non-bioabsorbable Class IIb

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
Imaging lesion localization marker implantable	Imaging lesion localization marker implantable	Class IIb
Submucosal injection needle	Submucosal injection needle	Class IIb
Urinary tract reconstructive material synthetic polymer non-bioabsorbable	Urinary tract reconstructive material synthetic polymer non-bioabsorbable	Class IIa
Urinary tract reconstructive material synthetic polymer non-bioabsorbable	Urinary tract reconstructive material synthetic polymer non-bioabsorbable	Class IIb