Prosthetic Leg Artificial Limb Polyurethane SACH Foot For Lower Limb Amputees  

Product name	Prosthetic Sach Foot
Item NO.	1F10(yellow)
Color	Beige, Brown
Size Range	21-30cm
Product weight	140g-650g
Load range	100-110kg
Material	Polyurethane/PU
Product description	1. They resemble the natural foot form and have a smooth surface and well-shaped toes. 2. The sach foot material adopt wood keel and polyurethane.
Main features	Lightweight, Beautiful and smooth appearance

    1. Company Profile .Business Type: Manufacturer/Factory .Main products:Prosthetic parts, orthotic parts .Experience:More than 15 years. .Management system：ISO 13485 .Location:Shijiazhuang, Hebei, China 2.Certificate:   ISO 13485/ CE/ SGS  MEDICAL I/II Manufacture certificat 3.Packing&shipment:  .The products firstly in a shockproof bag, then put into a small carton, then put into a normal dimension carton, Packing is suitable for the sea and air ship.   .Export carton weight: 20kgs.   .Export carton Dimension:   45*35*39cm   90*45*35cm   .FOB port:   .Tianjin, Beijing, Qingdao, Ningbo, Shenzhen, Shanghai, Guangzhou 4.Payment and Delivery .Payment Method:T/T, Western Union, Paypal, L/C .Delivery Tiem: within 3-5 days after receiving the payment. ㈠  Cleaning ⒈  Clean the product with a damp,soft cloth. ⒉  Dry the product with a soft cloth. ⒊  Allow to air dry in order to remove residual moisture. ㈡  Maintenance ⒈A visual inspection and functional test of the prosthetic components should be performed after the first 30 days of use. ⒉Inspect the entire prosthesis for wear during normal consultations. ⒊Conduct annual safety inspections. CAUTION Failure to follow the maintenance instructions Risk of injuries due to changes in or loss of functionality and damage to the product ⒈  Observe the following maintenance instructions. ㈢  Liability The manufacturer will only assume liability if the product is used in accordance with the descriptions and instructions provided in this document.The manufacturer will not assume liability for damage caused by disregarding the information in this document,particularly due to improper use or unauthorised modification of the product. ㈣  CE conformity This product meets the requirements of the European Directive 93/42/EEC for medical devices.This product has been classified as a class I device according to the classification criteria outlined in Annex IX of the directive.The declaration of conformity was therefore created by the manufacturer with sole responsibility acording to Annex VLL of the directive. ㈤  Warranty The manufacturer warrants this device from the date of purchase.The warranty covers defects that can be proven to be a direct result of flaws in the material,production or construction and that are reported to the manufacturer within the warranty period. Further information on the warranty terms and conditions can be obtained from the competent manufacturer distribution company.