Baxa repeater pump technical manual The following baxa repeater pump technical manual Pdf file begin with Intro. Product Code, with the device as opposed to the Operator. Repeater Pump model s 095, all customers received a CD containing a copy of the correct Operator Mannual. Pharmacy Pump Tube Set Repeater. Baxter H93811. Vented inlet spike and luer lock outlet for filling sterile oral dispensers luer syringes, vials, elastomeric infusers.

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Baxa Repeater Pump Technical Manual 2016

Baxa repeater pump manual pdf

Free Baxa Repeater Pump Manual

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Baxa Repeater Pump Technical Manual

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Class 2 Device Recall Repeater Pump
Date Initiated by FirmOctober 03, 2012
Date PostedOctober 25, 2012
Recall Status1Terminated 3 on February 15, 2013
Recall Event ID63379
System/device, pharmacy compounding - Product CodeNEP
ProductRepeater Pump, Class II device used for facilitating repeatable drug dosage distribution and reconstitution in hospital pharmacies. The device are Fluid Transfer Tube Sets, Sterile/EO, Std Volume Trifurcated, BAXA Corporation, Englewood, CO.
The Repeater Pump is a device that provides a peristaltic pump driven fluid transfer that facilitates repeatable drug dosage distribution and reconstitution in hospital pharmacies. The device is for use with IV bags, syringes, elastomeric infusers, and other drug administration containers.
Code InformationRepeater Pump model #s 095, 099, and 099R.
Recalling Firm/
Baxa Corporation
14445 Grasslands Dr
Englewood CO 80112-7062
For Additional Information Contact
The firm is issuing a field correction to the operators manual included with the 099 Repeater Pump because the Technical Manual was distributed with the device as opposed to the Operator Manual and the instruction for use contradict each other with regards to multiple source container use.
Packaging process control
Baxa Corporation sent a 'REPEATER PUMP PRODUCT NOTICE' to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. All customers received a CD containing a copy of the correct Operator Mannual, 5300-0754. Contact Technical Support at 800-678-2292 for questions regarding this notice.
Worldwide Distribution-USA (nationwide) and the countries of Argentina, Australia, Brazil, Canada, Columbia, Guam, Japan, Malaysia, Mexico, Panama, Puerto Rico, Taiwan, UK, and Venezuela.
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.