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 - Santa Barbara Imaging Systems

Address:

340 Storke Road Suite 101

Goleta

California 93117

United States

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Fibreoptic light cable Fibreoptic light cable Class I

Endoscope camera adaptor Endoscope camera adaptor Class I

Light source adaptor Light source adaptor Class I

Endoscopic video image processing unit Endoscopic video image processing unit Class I

Endoscopic device remote control Endoscopic device remote control Class I

Endoscope video camera Endoscope video camera 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
Fibreoptic light cable	Fibreoptic light cable	Class I
Endoscope camera adaptor	Endoscope camera adaptor	Class I
Light source adaptor	Light source adaptor	Class I
Endoscopic video image processing unit	Endoscopic video image processing unit	Class I
Endoscopic device remote control	Endoscopic device remote control	Class I
Endoscope video camera	Endoscope video camera	Class I