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

Back to MHRA

Manufacturer's Devices - ProSpon spol. s.r.o.

Address:

Jiího Voskovce 3206

Kladno

27201

Czechia

Authorised Representative/ UK Responsible Person
Name: Templar Regulatory Consulting Limited
Address:

11 Amor Way

Letchworth Garden City

Hertfordshire SG61UG

England United Kingdom

Code/Term Type

Proximal interphalangeal joint prosthesis one-piece Proximal interphalangeal joint prosthesis one-piece Class IIb

Orthopaedic surgical procedure kit non-medicated reusable Orthopaedic surgical procedure kit non-medicated reusable Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Proximal interphalangeal joint prosthesis one-piece	Proximal interphalangeal joint prosthesis one-piece	Class IIb
Orthopaedic surgical procedure kit non-medicated reusable	Orthopaedic surgical procedure kit non-medicated reusable	Class I