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ADM Night Use Ankle Foot Orthosis, Left or Right, for use with the ADM or the ADM External Rotation Bar

Single left or right. Only available from size 0 for use with ADM
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* Help? Foot Length Measurement Guide

A single (Left or Right side) night ADM Ankle Foot Orthosis (AFO) for use with Dobbs ADM Fixed External and Articulating External Rotation Bar Systems and/or with an Abduction Dorsiflexion Mechanism.

 

Advanced, modern and ultra low weight AFO to promote better clubfoot progression when using a Boots and Bar or ADM style brace.

 

 

 

ADM Modular System Overview

 

ADM Ankle Foot Orthosis (AFO)

 

ADM Abduction Dorsiflexion Mechanism

 

ADM Sole Kits and Footwear Adaption

 

Ambulatory ADM Product Overview

   

Dobbs ADM External Rotation Bars

 

ADM Ankle Foot Orthosis (AFO)

 

Dobbs ADM Fixed External Rotation Bars

 

Dobbs ADM Articulating External Rotation Bars

 

REGULATORY DETAILS    
CE logo  

ADM Modular Brace System

EU Declaration of Conformity

Dorsi Ramp

EU Declaration of Conformity

UK CA logo  

ADM Modular Brace System

UK Declaration of Conformity

Dorsi Ramp

UK Declaration of Conformity

FDA logo  

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

 

MHRA logo  

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

 

Veritas Logo  

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