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 - Xion GmbH

Address:

Pankstr.8

Pankstr.

Berlin

Berlin 13127

Germany

Authorised Representative/ UK Responsible Person
Name: DP Medical Systems Limited
Address:

15a Oakcroft Road

Chessington

Surrey KT9 1RH

England United Kingdom

Code/Term Type

Flexible video nasopharyngoscope Flexible video nasopharyngoscope Class IIa

Camera control unit Camera control unit Class I

Camera application software Camera application software

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
Flexible video nasopharyngoscope	Flexible video nasopharyngoscope	Class IIa
Camera control unit	Camera control unit	Class I
Camera application software	Camera application software