USB Programming Cable for PLC Controllers SLC 500 MicroLogix Series

$ 17.38

MPN: Does Not Apply Cable Length: 9.8ft/3m UPC: Does Not Apply Brand: Lolicute Item model number: USB-1747-CP3 gtin13: Does Not Apply

Description

Description: Enhance your PLC programming experience with our Replacement USB-1747-CP3 PLC Cable, expertly designed for SLC 5/03, 5/04, and 5/05 models, as well as Micrologix 1400 systems. This premium 9.8ft (3m) black cable ensures seamless connectivity and reliable performance, making it the perfect choice for engineers and technicians alike. The USB PLC Programming Cable allows easy communication with your controller, streamlining your programming tasks. Upgrade your setup today with this essential cable for unmatched convenience and efficiency! Packing List: -Package : 1* Programming Cable Product: Replacement USB-1747-CP3 PLC Cable Suitable for: SLC 5/03-5/04-5/05 SLC500 and Micrologix1400 Color: Black Length of Cable: 9.8ft/3m FDA Disclaimer: Statement:The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies. If so, do not bid on this item unless you are an authorized purchaser. If the item is subject to FDA regulation, I will verify your status as an authorized purchaser of this item before shipping of the item.(Seller name:May City:Beijing State:Beijing Country:China Phone :+86 18108119506 ) This item has been cleaned and treated according to the manufacturer's instructions. The Fingertip Pulse Oximeter is certified with the US FDA 510K No. K070371, the CE & TUV of Eureope and it is on the Australian Register of Therapeutic Goods (ARTG) with the code 136606. The Powered Surgical Instrument / Speed 808 System is certified with the US FDA 510(k) Number:K132989 The Powered Surgical Instrument / Hair Remove Device is certified with the US FDA 510(k) Number:K180353 The Powered Surgical Instrument / Hair Remove System is certified with the US FDA 510(k) Number:K141973 massager, vacuum, light induced heating / Slimming Treatment Device is certified with the US FDA 510(k) Number:K161892