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Draeger Babylog Vn500 Technical Manual Download
The Babylog® VN500 combines our years of experience with the latest technology. The result is a complete, integrated ventilation solution for the tiniest of patients. Move on toward new frontiers today and be prepared for the developments of tomorrow. D- The Babylog® VN500 with Infinity® Medical Cockpit™ C500 D. Draeger Babylog VN500 Product Trainer. Drager Babylog 8000 Plus Service Manual; Drager Babylog Vn500 User Manual Drager Babylog 8000 Plus Service Manual. Any assistance would be greatly appreciated. Robyn Acting Nurse Educator SCBU. Netsupport trial period expired for mac. Babylog Vn500 User Manual Marshall Kirkland. Drager Ventilator Training - Duration. Drager Babylog VN500. Drager - Babylog 8000+Ventilation in harmony.
Draeger Babylog Vn500 Technical Manual 2017
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Drager Vn500 User Manual
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Drager sent an Urgent Medical Device Recall letter dated February 2014. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to use an affected device for patient transport only if absolutely necessary; not to rely on the battery charge status indicator, always supervise the patient and the ventilator during transport; ensure that they have a manual breathing bag available for manual ventilation as recommended in the instructions for use. If the power fail alarm occurs during transport, immediately provide manual ventilation and connect ventilator to a wall power source to resume ventilation. DragerService representative will schedule the implementation of a permanent solution as quickly as possible. The letter should be distributed to users of the Evita V500 and /or Babylog VN500 Ventilators to make them aware of this device behavior and risk mitigation measures. Customers with questions were instructed to call 1-800-543-5047. For questions regarding the operation and/or servicing of their Draer ventilator contact Technical Support at 1-800-543-5047. For questions regarding this recall call 215-721-5400. | |||||||||||||||||||||||||||
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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 = CBK and Original Applicant = DRAEGER MEDICAL AG & CO. KG 510(K)s with Product Code = CBK and Original Applicant = DRAGER MEDICAL AG & CO. KGAA |