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 - FFDM TIVOLY

Address:

78-80 Avenue de la Prospective

18 020 Bourges Cedex

18 020 Bourges Cedex

France

Authorised Representative/ UK Responsible Person
Name: Panadent Limited
Address:

149 sevenoaks way

Orpington

Kent BR5 3AQ

United Kingdom

Code/Term Type

Margin finishing dental file/rasp reusable Margin finishing dental file/rasp reusable Class I

Manual endodontic file/rasp reusable Manual endodontic file/rasp reusable 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
Margin finishing dental file/rasp reusable	Margin finishing dental file/rasp reusable	Class I
Manual endodontic file/rasp reusable	Manual endodontic file/rasp reusable	Class I