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 - Baholzer Endoskopie GmbH & Co.KG

Address:

Neckartal 100

Rottweil

78628

Germany

Authorised Representative/ UK Responsible Person
Name: Kelyon Ltd
Address:

The Maltings East Tyndall Street Cardiff Bay

Cardiff

CF24 5EA

Wales United Kingdom

Code/Term Type

Flexible fibreoptic epiduroscope Flexible fibreoptic epiduroscope 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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