Advia Centaur Cp User Manual Pdf

Posted : admin On 12/21/2021
  1. Advia Centaur Xp User Manual Pdf
  2. Advia Centaur Cp User Manual
  3. Advia Centaur Xp Manual Pdf
  • Siemens ADVIA 1800 Manuals Manuals and User Guides for Siemens ADVIA 1800. We have 1 Siemens ADVIA 1800 manual available for free PDF download: Operator's Manual. Siemens ADVIA 1800 Operator's Manual (222 pages) Chemistry system.
  • Performance evaluation of Siemens ADVIA Centaur (R) enhanced estradiol assay and a split sample comparison with liquid chromatography-tandem mass spectrometry.
  • ADVIA Centaur Immunoassay Systems Outside the U.S. Assay menu Allergy Total IgE Anemia/Iron Metabolism Ferritin 1 Folate RBC Folate Vitamin B12 Bone Metabolism Vitamin D Total 1 Cardiac BNP CKMB D-Dimer 1 Galectin-3 1 Myoglobin Tnl-Ultra®.
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The ADVIA Centaur® XP system is an automated, immunoassay analyzer that offers optimal productivity and efficiency. In this online training program, you'll learn about the components of the instrument, navigate the software and routine operation.  You'll also learn about additional concepts including calibration, quality control, maintenance and troubleshooting. ADVIA Centaur Immunoassay Systems Outside the U.S. Assay menu Allergy Total IgE Anemia/Iron Metabolism Ferritin 1 Folate RBC Folate Vitamin B12 Bone Metabolism Vitamin D Total 1 Cardiac BNP CKMB D-Dimer 1 Galectin-3 1 Myoglobin Tnl-Ultra®.

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VACUUM PUMP 572703B P/N: 078-B050-02 REV.B VP FOR ADVIA CENTAUR XP AND CLASSIC
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SIEMENS ADVIA CENTAUR CP SAMPLE RACKS 100MM PART NUMBER 10320160 USED
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SIEMENS ADVIA CENTAUR CP SAMPLE RACKS 100MM PART NUMBER 10320160
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SIEMENS CENTAUR CP PROBES ASSY REAGENT WITH TUBING 10810324
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Advia Centaur Xp User Manual Pdf

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Advia Centaur Cp User Manual

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Advia Centaur Xp Manual Pdf

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Class 2 Device Recall ADVIA Centaur TnIUltra
Date Initiated by FirmMay 19, 2015
Date PostedJuly 23, 2015
Recall Status1Terminated 3 on July 17, 2019
Z-2207-2015
Recall Event ID71337
K053020
Immunoassay method, troponin subunit - Product CodeMMI
ProductADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests
Product Usage:
For in vitro diagnostic use in the quantitative determination of cardiac troponin I (cTnl) in serum, heparinized plasma, or EDTA plasma using the ADVIA Centaur/ADVIA Centaur XP/ADVIA Centaur XPT/ADVIA Centaur CP systems. Cardiac troponin I determinations aid in the diagnosis of acute myocardial infarction and in the risk stratification of patients with non-ST segment elevation acute coronary syndromes with respect to relative risk of mortality, myocardial infarction (MI) or increased probability of ischemic events requiring urgent revascularization procedures.
Code Information***This field action applies to all in-date lots of reagents (Kit lots ending in 088, 089, 090, 091, 093 and 094) and all future lots until the issue is resolved and a follow-up communication is issued by Siemens.**** SMN 10317708 - 100 tests 43796099 May 25, 2015 43818088 May 25, 2015 44793088 May 25, 2015 45687089 June 22, 2015 46527089 June 22, 2015 48096089 June 22, 2015 49216090 August3, 2015 50779090 August3, 2015 52113091 September 14, 2015 53091093 October 19, 2015 54684093 October 19, 2015 SMN 10317709 -500 tests 43797088 May25, 2015 43819088 May25,2015 44098088 May25, 2015 44623088 May 25, 2015 45688089 June 22, 2015 46661089 June 22, 2015 48301090 August3, 2015 49869090 August 3, 2015 50884091 September 14, 2015 51471091 September 14, 2015 51798091 September 14, 2015 53092093 October 19,2015 53231093 October 19,2015 54742094 December 6, 2015
Recalling Firm/
Manufacturer
Siemens Healthcare Diagnostics, Inc
333 Coney St
East Walpole MA 02032-1516
For Additional Information Contact
508-660-4381
System-to-system bias between the Tni-Ultra assay on the ADVIA Centaur CP and ADVIA Centaur/ADVIA Centaur XP/ADVIA Centaur XPT systems.
Under Investigation by firm
Siemens sent an Urgent Medical Device Correction letter dated via Federal Express to affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to complete and return the Field Correction Effectiveness Check attached to the letter. For questions contact your Siemens Customer Care Center or your local Siemens technical support representative.
SMN10317708 = 20544 kits & SMN 10317709 = 21159 kits
Worldwide distribution - US Nationwide in the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MN, MS, MT, NC, NJ, NM, NY, NV, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WY, WV, and Puerto Rico; and the countries of Algeria, Austria, Bahrain, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Egypt, Estonia, Finland, France, Georgia, Germany, Great Britain, Greece, Hungary, Iceland, Indonesia, Ireland, Italy, Jordan, Latvia, Lebanon, Lithuania, Luxembourg, Macedonia, Malta, Morocco, Netherlands, Norway, Pakistan, Poland, Portugal, Qatar, Romania, Russian Federation, Saudi Arabia, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Tunisia, Turkey, United Arab Emirates, AR, AU, BD, BR, CA, CL, CN , CO, CR, DO, EC, HK, ID, IE, IL, IN, JP, KR, LK, MX, MY, NI, NP, NZ, PE, PH, PY, SA, SG, TH, TW, UY, VN, and ZA.
TPLC Device Report
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) Database510(K)s with Product Code = MMI and Original Applicant = BAYER HEALTHCARE, LLC