Smiths Medical 21-2120-0102-51 - CADD-Solis VIP Ambulatory Infusion Pump, Each
Smiths Medical 21-2120-0102-51 CADD-Solis VIP Ambulatory Infusion Pump
The CADD-Solis VIP (variable infusion profile) Ambulatory Infusion Pump is designed to facilitate patient care for a variety of adult and pediatric patients and clinical care areas. The pump can be programmed with a protocol configuration consisting of a therapy, qualifier and drug information. The pump delivers via the following delivery profiles: PCA, continuous, intermittent, variable stepped rate, and tapered infusions for analgesia, chemotherapy, hydration, antibiotics, immune globulin, and TPN.
CADD-Solis Medication Safety Software Administrator Program: Administrator software is a Windows based application used by select staff members to create and manage the standardized pump protocols. The application is used to securely program the CADD-Solis VIP pump saving Pharmacist and Nursing time in manually programming the infusion pump. Infusion data is collected for additional pump documentation, reporting and CQI data analysis.
Smiths Medical 21-2120-0102-51 CADD-Solis VIP Ambulatory Infusion Pump Benefits
- Developed with reliable CADD pump technology that meets industry standards for infusion pumps
- The patient-focused user interface may help reduce training time by providing therapy related information in an easy to understand format
- Graphs and reports provide trending data and delivery history for patient assessment and continuous quality improvement.
Advantages of the Smiths Medical 21-2120-0102-51 CADD-Solis VIP Ambulatory Infusion System
Patented help screens
Patented help screens assist with troubleshooting, if alarms occur, to help reduce clinician field visits
Differentiated alarms by color and sound with high (red), medium (amber) and low (blue) priority
On-board reports provide trending data and simple patient assessments
Device Characteristics of Smiths Medical 21-2120-0102-51 CADD-Solis VIP Ambulatory Infusion Pump
|What MRI safety information does the labeling contain?||Labeling does not contain MRI Safety Information|
|Device required to be labeled as containing natural rubber latex or dry|
natural rubber (21 CFR 801.437):
|Device labeled as "Not made with natural rubber latex":||No|
|Prescription Use (Rx):||Yes|
|Over the Counter (OTC):||No|
|Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):||No|