C-Pro Direct. Ambulatory ADM Footwear Adaption Kit without Soles (single sole)

Ambulatory ADM Footwear Adaption Kit without Soles (single sole)

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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:

ADM Sole Plug
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 best undertaken using a computer numerically controlled routing machine.

REGULATORY DETAILS
		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

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