Ambulatory ADM Footwear Adaption Kit with Soles (single sole)

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£26.00
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A kit of parts to enable a trained Orthotic and Prosthetic (O&P) technician to adapt footwear to connect to an Abduction Dorsiflexion Mechanism (ADM).  The kit provides all the essential parts necessary to undertake the adaption.

The kit comprises:

  • Upper Sole
  • Lower Sole
  • ADM Socket
  • Dummy Side Clip
  • Ferrules (x2)
  • Clip Removal Tool (x2)

Size Guide

Foot Length (mm)

Size

ADM Compatibility

<= 132

Small

XXXs to Small

133 to 202

Large

Small-Medium to Large

203 to 252

Extra Large

Extra Large

Note:

Footwear adaption using the Footwear Adaption Kit (with soles) can be undertaken using just the tools and techniques common to most O&P workshops.  Footwear adaption using the Footwear Adaption Kit (without soles) requires the ability to route a defined recess into the sole of the footwear.  This is normally undertaken using a computer numerically controlled routing machine.

A kit of parts to enable a trained Orthotic and Prosthetic (O&P) technician to adapt footwear to connect to an Abduction Dorsiflexion Mechanism (ADM).  The kit provides all the essential parts necessary to undertake the adaption.

The kit comprises:

  • Upper Sole
  • Lower Sole
  • ADM Socket
  • Dummy Side Clip
  • Ferrules (x2)
  • Clip Removal Tool (x2)

Size Guide

Foot Length (mm)

Size

ADM Compatibility

<= 132

Small

XXXs to Small

133 to 202

Large

Small-Medium to Large

203 to 252

Extra Large

Extra Large

Note:

Footwear adaption using the Footwear Adaption Kit (with soles) can be undertaken using just the tools and techniques common to most O&P workshops.  Footwear adaption using the Footwear Adaption Kit (without soles) requires the ability to route a defined recess into the sole of the footwear.  This is normally undertaken using a computer numerically controlled routing machine.

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