Bd Bactec Fx 40 User Manual
Posted : admin On 01.06.2020- BD BACTEC™ FX40 Instrument. The BD BACTEC FX40 blood culture instrument is a modular, affordably-priced system that offers lower volume customers the opportunity to access the state-of-the-art workflow and performance of the BD BACTEC FX system.
- Jun 14, 2014 BD BACTEC FX40 Blood Culture Instrument Now Communicates with the BD EpiCenter Data Management System. Product News Jun 14, 2014. The BACTEC FX and the BD BACTEC 9000 families of continuous monitoring blood culturing instruments offer performance, safety, reliability, ease of use, media quality and service to meet the needs of today's top.
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Windows 10 language pack manual download. Mar 25, 2019 BD BACTEC FX40 CERTIFICATION TRAINING MANUAL 1. BD BACTEC™ FX and BD BACTEC™ FX40 Certification Training Manual Tier I, II and III BD Diagnostics Technical Services and Support 7 Loveton Circle Sparks, MD 21152 Phone: 800-638-8663 E-mail: technicalservices@bd.com.
Bactec Fx40 User Manual
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Bactec Fx Instrument Manual
Bd Bactec Fx40 User Manual Pdf
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| Nonconforming Material/Component | |||||||||||||||||||||||||||
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| BD Diagnostics initiated a field correction by phone on December 9, 2013, to affected customers and followed the calls with letters, e-mails, or fax. BD Diagnostics sent a secondary Urgent Field Corrective Action letter dated November 2013 to all affected customers. The recalling firm Secondary notifications were serial number specific and explained that some BD BACTEC FX instruments contain racks that may demonstrate variable indicator light intensities. Specifically, the Anonymous vial indicator lights which should appear yellow may instead appear more green in color. BD noted that affected instruments continue to function properly and will not report an incorrect result. The issue is limited to the yellow indicator lights only. Red and green indicator lights appear as intended. BD is developing software to correct this issue and anticipates that the new software will be available to begin instrument updates by February, 2014. The new software will not affect instrument if the indicator lights are functioning as intended. Until the software can be updated on your instrument, BD provided workflow instructions to ensure that the indicator light issue does not occur. For questions regarding this recall call 410-316-4054. | |||||||||||||||||||||||||||
| 2 units | |||||||||||||||||||||||||||
| Worldwide Distribution - USA (nationwide) and Internationally to IN, AU, CN, AR, BE, PE, KR, BR, CO, SG, TH, BN, HK, JP, and CA. | |||||||||||||||||||||||||||
| 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) Database | 510(K)s with Product Code = MDB and Original Applicant = BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC | ||||||||||||||||||||||||||