- Baxter Homechoice User Manual
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- Homechoice Pro Automated Pd System User Manual For Self Testing
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Baxter Homechoice User Manual
‘HOME CHOICE’ AUTOMATED PERITONEAL DIALYSIS B) BAG CONNECTION 1. Wash hands for 3 Minutes (hands & arms) and rinse; then wash hands again. Remove coloured ring pull from bag. Remove clear line protector from the machine line (do the red clamp line first) and screw the machine line into the bag. HOMECHOICE PRO and HOMECHOICE Automated Peritoneal Systems Product Description Pack Factor Price Devices 5C4471 HOMECHOICE Automated PD System 1/each $17,719.67 5C8310 HOMECHOICE PRO Automated PD System 1/each $20,251.06 HOMECHOICE PRO System HOMECHOICE System Luer Disposable Sets R5C4479C Automated PD Set with Cassette - 4 Prong 30/case $966.63. Sep 14, 2018 Baxter Homechoice Pro Home Apd Automated Peritoneal Dialysis Machine - Source: www.ebay.com. Software Version Homechoice Pro Apd Systems - Source: docplayer.net. Baxter home dialysis machine amia baxter homechoice manual baxter s homechoice apd system bringing the clinic to your patients baxter renal care.
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Iep Direct
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Homechoice Pro Automated Pd System User Manual For Self Testing
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The firm, Baxter, sent an 'IMPORTANT PRODUCT INFORMATION' letter dated October 6, 2014 to all peritoneal dialysis provider direct accounts. Baxter also sent an 'IMPORTANT PRODUCT INFORMATION' letter dated October 9, 2014 to all peritoneal dialysis patient direct accounts The letters described the product, problem and actions to be taken. The letters included instructions for the recipients to complete the attached Customer Reply Form and to return it to Baxter via scanned e-mail to: [email protected] or fax : 224-270-5457. In addition, the letter to patients instructed them to contact their healthcare provider to discuss this issue. Customers with clinical questions should contact Baxter's Renal Division Clinic Helpline at 888-736-2573, option 2 (8:00 AM - 5:00 PM CST). Adverse reaction or quality problems experienced with the use of these product can be reported by contacting Baxter Product Surveillance at 800-437-5176 (Monday - Friday, 8:00 AM - 5:30 PM CST) or e-mail to [email protected]. Customers with general questions about the letter should contact The Center for One Baxter at 800-422-9837 (Monday - Friday, 8:00 AM - 5:00 PM CST). | |||||||||||||||||||||||||||
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Worldwide Distribution: US (nationwide) Including states of: AK, AL, AR, AZ, CA, CO, CT, DE, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and District of Columbia; and countries of: Algeria, Argentina, Aruba, Australia, Austria, Bahamas, Bahrain, Barbados, Belarus, Belgium, Bosnia, Brazil, Bulgaria, Cayman Islands, Chile, Colombia, Croatia, Cuba, Czech Republic, Denmark, Ecuador, Egypt, El Salvador, Estonia, Finland, France, Georgia, Germany, Greece, Guatemala, Honduras, Hong Kong, Hungary, India, Iran, Iraq, Ireland, Israel, Italy, Jamaica, Japan, Jordan, Kazakhstan, Kuwait, Lebanon, Macedonia, Malaysia, Malta, Mexico, Morocco, Netherlands, New Zealand, Nicaragua, Norway, Oman, Panama, Poland, Portugal, Quatar, Romania, Russia, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, United Arab Emirates, United Kingdom, and Venezuela. | |||||||||||||||||||||||||||
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55. | |||||||||||||||||||||||||||
510(K) Database | 510(K)s with Product Code = FKX and Original Applicant = BAXTER HEALTHCARE CORP. |