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 screensPatented help screens assist with troubleshooting, if alarms occur, to help reduce clinician field visits |  |
Differentiated alarmsDifferentiated alarms by color and sound with high (red), medium (amber) and low (blue) priority |  |
On-board reportsOn-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): | No |
| Device labeled as "Not made with natural rubber latex": | No |
| For Single-Use: | No |
| Prescription Use (Rx): | Yes |
| Over the Counter (OTC): | No |
| Kit: | No |
| Combination Product: | No |
| Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P): | No |
