5.0Mhz Micro Convex Probe FOR CONTEC CMS600P2 Digital Ultrasound Scanner Description 5.0Mhz Micro Convex Probe is for Contec Ultrasound Scanner CMS600P2 or CMS600P1,Please confirm this before you order,thanks very much! Note: Only Probe, not including Ultrasound scanner!!! Shipping ? 1. For your earlier and safer to receive the item, please leave us your detailed address and telephone number for posting the item. ? 2. Your item will be sent via small parcel within 48 hours after payment is received. The shipping time may is around 15-45days. ? 3. As the usual way, the buyers are responsible for the duties, taxes or other VAT or extro charges from the import countries. ? 4. All items will be shipped to buyer's PayPal address. Please confirm your PayPal address is correct before purchase. ? 5.It's international shipping andAirmail is cheapest post way, so it will take a long time for delivery. If you don't want to wait so long time, please pay the Express fee or don't buy it. Terms of Sale There are not extra taxes, VAT or other unmentioned payment. You pay us with goods subtotal + shipping cost (not include duties). But you need to pay for the import duties in case that occurred for certain goods, or you may kindly give us some suggestions about that, we promise to do our best to help you! Feedback Feedback:please leave me a positive feedback if you are satisfied with our products, Your positive feedback will be appreciated very much,thank you very much! If you have any problems, please contact us as soon as possibel before you open a case and leave a negative feedback or ship the item back, we promise we will give you a satisfied answer, thank you for your understanding! Return - After service We offer 14 days return policy. 100% satisfaction is our goal! 1.All items are brand new ,with 1years warranty. 2.If you have a defective item, you want to return or discount. Please contact us within 2 days from you receive the shipment. 3.We will refund the money to you when we get the return items or replace item for you. 4. All return items must be returned with it's original packaging and accessories. Customer is responsible for shipping charges on returned items. International Buyers - Please Note: ? Import duties, taxes and charges are not included in the item price or shippingcharges. These charges are the buyer's responsibility. ? Please check with your country's customs office to determine what these additional costs will be prior to bidding/buying." The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923, and certified by FDA of United States and CE,TUV of Europe. The Fingertip Pulse Oximeter that is FDA 510K Approved Payment 1. Paypal, paypal account 2.The payment are expected within 7 business days after the last winning auction is closed. About Us Contec Medical Systems focusing on research, manufacture and distribution of medical instruments,was founded in 1992 as a high-tech company. At present there are more than 1200 employees in our company.Our product line covers a wide range of 13 categories. Most of the domestic hospitals are our customers. Contec hopes to cooperate with international companies to supply more innovative design and advanced technology products We sincerely welcome you to become one of our global partners.We are looking forward to establishing a successful business relationship with you. Contact Us Contact Person :Tessy Skype:contec.tessy Tel: 86-335-8015594 Fax:86-335-8015590 Contec Medical Systems Co.,Ltd, Manufacturer, Qinhuangdao, China Address: No.112 Qinhuang West Avenue, Qinhuangdao Economic and Technical Development Zone, Hebei Province, China Buy Safe Product! The following FDA Disclaimer is required for all eBay listing in Healthcare category and is included for REFERENCE: 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 the item is subject to FDA regulation, We will verify your status as an authorized purchaser of this item before shipping of the item. FDA K Number CMS50C Pulse Oximeter Premarket Submission Number(510K): K073454 Listing Number: D045684 CMS50D/L/DL Pulse Oximeter Premarket Submission Number(510K): K082641 Listing Number: D064765 Sonoline A/B, Baby Sound A/B Pocket Fetal Doppler Premarket Submission Number(510K): K082480 Listing Number: D072247 CMS50E, CMS50F, CMS60C, CMS60D Pulse Oximeter Premarket Submission Number(510K): K090671 Listing Number:D078664 ECG80A ECG machine Premarket Submission Number(510K): K090936 Listing Number: D081157 If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA's Center for Devices and Radiological Health. Buy Safe Product! The following FDA Disclaimer is required for all eBay listing in Healthcare category and is included for REFERENCE: 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 the item is subject to FDA regulation, We will verify your status as an authorized purchaser of this item before shipping of the item. FDA K Number CMS50C Pulse Oximeter Premarket Submission Number(510K): K073454 Listing Number: D045684 CMS50D/L/DL Pulse Oximeter Premarket Submission Number(510K): K082641 Listing Number: D064765 Sonoline A/B, Baby Sound A/B Pocket Fetal Doppler Premarket Submission Number(510K): K082480 Listing Number: D072247 CMS50E, CMS50F, CMS60C, CMS60D Pulse Oximeter Premarket Submission Number(510K): K090671 Listing Number:D078664 ECG80A ECG machine Premarket Submission Number(510K): K090936 Listing Number: D081157 If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA's Center for Devices and Radiological Health. Buy Safe Product! The following FDA Disclaimer is required for all eBay listing in Healthcare category and is included for REFERENCE: 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 the item is subject to FDA regulation, We will verify your status as an authorized purchaser of this item before shipping of the item. If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA's Center for Devices and Radiological Health. The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923, and certified by FDA of United States and CE,TUV of Europe. The Fingertip Pulse Oximeter that is FDA 510K Approved
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