The Abbot CELL-DYN® 1800 Hematology Analyzer is designed to meet the the demands of almost any laboratory. The Cell-Dyne 1800 is a quick and accurate system that allows convenient access to patient results through its advanced onboard data management system. With an aspiration volume of only μL, this small system can fit under any standard physicians office laboratory cabinet. The Cell-dyn 1800 Hematology Analzyers can handle up to 10,000 samples with the expanded data management system. It incorporates a 3-part differential and 18 parameter blood count. An optional bar code ready may be use to eliminate transcription data entry errors.
Cell Dyn 3200 Cs Service Manual If searched for the ebook Cell dyn 3200 cs service manual in pdf format, in that case you come on to the faithful website. The CELL-DYN 3200 is a multi-parameter automated hematology analyzer designed for in vitro diagnostic use in clinical laboratories. The analyzer incorporates.
Data may be out put to both ink jet and dot-matrix printers. The Cell-Dyn 1800 uses only 3 reagents including cyanide-free differential lyse that reduces bio-hazards and reduces safety risks. The key benefits of the Cell-Dyn 1800 include:. Simple Operation.
Accurate 3-part differential analysis. Reliability all in a single bench-top unit The CELL-DYN® 1800 Hematology Analyzer is the latest 3-part differential analyzer based on the proven technology used since the founding of the CELL-DYN® line. Offering 16 parameters and extensive QC and data management capabilities, the CELL-DYN 1800 meets the needs to today's growing labs. The CELL-DYN 1800 is smaller than its predecessors and fits in standard physicians laboratories.
The system utilizes impedance resistance to measure human cells while incorporating the patented von Behrens plate to reduce coincidence counts from each sample. Copyright © 2018 GMI. This page and all associate pages from all years (and their HTML) of this website and all contents at www.gmi-inc.com are the sole property of GMI OpCo LLC (dba GMI) & GMI and are protected by GMI OpCo LLC (GMI hereafter) copyright protection laws and may not be reproduced in any form nor may any content or any images be copied, removed, or linked-to without the owners express written permission. All instruments mentioned in our website are the trademarks of their respective manufacturer. GMI makes no claims of special affiliation with or special sanctions by the original manufacturers or their respective trademarks.
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ABBOTT LABORATORIES CELL-DYN 3200 CS 110V AUTOMATED HEMATOLOGY ANALYZER Catalog Number 4H59-01 Device Problems Other (for use when an appropriate device code cannot be identified); Incorrect Or Inadequate Test Results Event Date Event Type Malfunction Manufacturer Narrative Investigation summary: the customer states that platelet results were generated using a cell-dyn 3200 cs analyzer that were different than platelet results obtained from a reference lab (platform= coulter). The customer performed all required maintenance and performed precision, calibration and calibration verification. All were within specification. Controls for three levels recovered within range. The customer then ran a comparison study using five normal specimens and found that the platelet results generated by the cell-dyn 3200 were higher than the customer's other cd 3200 and also higher than results from the reference lab's analyzer.
A field service rep (fsr) contacted the customer on 2/22/2008 and calculated a new calibration factor for the customer, and had the customer adjust the calibration factor then run precision and controls obtaining values within specification. Trending: a review of complaint reports for the period of june 2007 through january 2008, did not indicate any adverse trend for the cell-dyn 3200 for the complaint issue. The event is addressed in the cell-dyn 3200 system operator's manual, 06h60-01, rev. M under maintenance.
Troubleshooting and diagnostics sections of the manual. Conclusion: the analyzer involved in the issue was evaluated. The analyzer was calibrated to resolve the issue. Verification tests were performed with results acceptable. There was no further impact to pt management reported due to this issue.
This is the final report. Event Description The customer states that discrepant platelet results were generated using a cell-dyn 3200 cs analyzer that were reported out of a lab and questioned by a physician. Pt chemotherapy doses were adjusted based on the reported platelet results.
Testing at a reference lab obtained platelet results that were higher than those generated by the lab using the cell-dyn 3200 sl analyzer. There was no further impact to pt management reported. Brand Name CELL-DYN 3200 CS 110V Type of Device AUTOMATED HEMATOLOGY ANALYZER Manufacturer (Section D) ABBOTT LABORATORIES 5440 patrick henry dr.
Santa clara CA 95054 Manufacturer Contact sudarshan hebbar, md, d-3mqc, ap6b 100 abbott park rd abbott park, IL MDR Report Key 1019176 Report Number 29-00472 Device Sequence Number 1 Product Code Report Source Manufacturer Source Type Consumer,Health Professional Reporter Occupation Other Type of Report Initial Report Date 1 Device Was Involved in the Event 1 Patient Was Involved in the Event Date FDA Received Is This An Adverse Event Report? Yes Is This A Product Problem Report? Yes Device Operator Health Professional Device Catalogue Number 4H59-01 Was Device Available For Evaluation? Yes Is The Reporter A Health Professional? Yes Date Manufacturer Received Was Device Evaluated By Manufacturer? Yes Date Device Manufactured Is The Device Single Use?
Service Manual Cell Dyn 3200 Price
No Is this a Reprocessed and Reused Single-Use Device? No Type of Device Usage Unkown Patient TREATMENT DATA Date Received: Patient Sequence Number: 1 Treatment CD32K DILUENT/SHEATH REAGENT LIST NO. 3H79-01 LOT NO.