C-Pro Direct. ADM Night Use Ankle Foot Orthosis, Left or Right, for use with the ADM or the ADM External Rotation Bar

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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A single ADM night use ankle foot orthosis (AFO) for use with the ADM or the ADM External Rotation Bar.

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 ADM Ankle Foot Orthosis (AFO) 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

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