Replacement Strap Pads

ADM Modular Brace System

EU Declaration of Conformity

Dorsi Ramp

EU Declaration of Conformity

ADM Modular Brace System

UK Declaration of Conformity

Dorsi Ramp

UK Declaration of Conformity

Search the FDA Establishment Registration and Device Listing Database using

For C-Pro Direct:

Owner operator number:  10040405 or 

Registration number:  3009097552

For Kiddfoot:

Owner operator number:  10084074

Registration number:  3021014441

C-Pro Direct Ltd is a UK manufacturer of Medical Devices and is registered with the MHRA.  Registration number 5447.  Details of the registration are available on the MHRA Public Access Registration Database by searching for C-Pro Direct Ltd

C-Pro Direct is UKAS certified by NQA to the Medical Device Manufacturing Standard ISO 13485

Click here to download a copy of our registration

C-Pro Direct Ireland Limited is a wholly owned subsidiary of the UK company C-Pro Direct Ltd and is registered with the HPRA in Ireland as the Authorised Representative, Importer and Distributor for C-Pro Direct products.

EUDAMED Registrations

C-Pro Direct is registered on EUDAMED.  The details can be found on the EUDAMED public access database and searching using the Actor / SRN numbers given below.

C-Pro Direct Ltd (UK) is registered on EUDAMED as the Manufacturer with the Single Registration Number:

GB-MF-000025827

C-Pro Direct Ireland Limited is registered on EUDAMED as the Authorised Representative with the Single Registration Number:

IE-AR-000019792

C-Pro Direct Ireland Limited is registered on EUDAMED as the Importer with the Single Registration Number:

IE-IM-000023320