C-Pro Direct. Non-Ambulatory ADM, Unilateral including Night Orthosis

Non-Ambulatory ADM, Unilateral including Night Orthosis

Non-Ambulatory ADM, Unilateral, left or right including left or right Night Orthosis

Foot Length (L in mm) Help?

Lower Leg Length (P in mm) Help?

STJ Abduction Spring *

TTJ Dorsiflexion Spring *

Which foot is the ADM AFO sandal required for *

Confirm approval for patient use of ADM *

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Name of clinician approving patient use of ADM *

ADM Product Code

Sandal Product Code

Quantity:

Overview
Instructions
More Information
Size Guide

Single ADM Device and night use AFO (sandal). Comprises 1 ADM device and 1 AFO (sandal):

See Product Overview and Advantages documents for more details:

		ADM Modular System Overview Czechia_CS English_EN French_FR German_DE Italian_IT Polish_PL Portuguese_PT Russian_RU Spanish_ES Turkish_TR
		Advantages of the ADM Modular Brace System Czechia_CS English_EN French_FR German_DE Italian_IT Polish_PL Portuguese_PT Russian_RU Spanish_ES Turkish_TR

INSTRUCTIONS FOR USE
		Instructions for Use Abduction Dorsiflexion Mechanism (ADM) 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
		Instructions for Use Ambulatory Abduction Dorsiflexion Mechanism (ADM) 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

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 certified by Bureau Veritas to the Medical Device Manufaturing 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

ADM Modular System Size and Selecton Guide

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