NHS Code
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The must have accessories for busy clubfoot clinics needing to operate at maximum efficiency.
Bar and Clip Boxes are part of the ADM Modular Brace System Clinic Accessories range used to establish and organise a stock of ADM Modular System Bar and Clip components. The Large Fixed Bar Clip Box provides 4 Left and 4 Right Small Fixed Bar Clips, 3 complete Kits of Bars (18 Bars) and 6 Bar Clip Removal Tools in an stackable organiser box.
Once you have established and organised your stock of ADM Modular Brace System items it is easy to order top-up stock as and when required. See the Bulk Ordering page.
Bar Clip Box and Sizing Liners
ADM Modular System Overview
ADM Ankle Foot Orthosis (AFO)
ADM Abduction Dorsiflexion Mechanism
ADM Sole Kits and Footwear Adaption
Ambulatory ADM Product Overview
ADM Modular Brace System Clinic Accesories
Dobbs ADM External Rotation Bars
Dobbs ADM Fixed External Rotation Bars
Dobbs ADM Articulating External Rotation Bars
Two size options; Small and Large. Each option has 3 possible clip configurations to cater for clinics that use both 70 degree and 60 degree clips on affected clubfeet or just one of these.
Box Contents
Instructions for UseADM External Rotation Bar (ERB)English: English
Images: Images only (use with Sets 1 to 4 below)
Set 1: Germany, Italy, Sweden, Netherlands, France, Poland
Set 2: Ireland, Spain, Czechoslovakia, Norway, Denmark, Slovak
Set 3: Greece, Portugese, Bulgarian, Lithuanian, Finland
Set 4: Slovenia, Croatia, Latvia, Sebian, Estonian, Hungarian
Set 5: Malta, Russia, Arabic, Turkey, Japan
Symbols Used in IFU
ADM Modular Brace System
EU 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
Choose your country:
Note: Limited product availability in US Dollars.
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