Product Description
Avanos Medical PM045-A - ON-Q Pain Relief System with Dual SILVERSOAKER Antimicrobial Catheters, 270 ml x 4 ml/hr (2ml/hr + 2ml/hr), 10 in. (25 cm), 5/Case
Avanos Medical PM045-A - ON-Q Pain Relief System with Dual SILVERSOAKER Antimicrobial Catheters
The ON-Q Fixed Flow Pump Kits With ON-Q SilverSoaker Catheter is a non-narcotic pain relief system which continuously delivers a regulated flow of local anesthetic to a patients surgical site or in close proximity to nerves, providing targeted pain relief for up to 3-5 days.The ON-Q Fixed Flow Pump comes in a variety of pump sizes and flow rate. It comes with a SilverSoaker catheter designed with a hollow fiber which allows for even distribution of local anesthetic through the soaker infusion segment. As with the pump, the SilverSoaker catheter comes in a variety of soaker infusion lengths for different lengths of incision. The SilverSoaker* has an additional silver coating that works as an anti-microbial agent. In addition, the SilverSoaker catheter comes with depth markers for placement guidance.
Avanos Medical PM045-A - ON-Q Pain Relief System with Dual SILVERSOAKER Antimicrobial Catheters Features & Benefits
- Can provide non-narcotic, targeted pain relief for up to 3-5 days
- The ON-Q Fixed Flow Pump is available in a variety of fill volumes and flow rate options
- Comes with a SilverSoaker* catheter designed to provide even distribution of local anesthetic
- The SilverSoaker catheter comes with an additional silver coating that works as an anti-microbial agent
- The SilverSoaker catheter is designed with depth markers for accurate placement
Avanos Medical PM045-A - ON-Q Pain Relief System with Dual SILVERSOAKER Antimicrobial Catheters Specifications
| Made With DEHP | Yes |
| Single Use | True |
| Sterile | Yes |
| Sterilization Method | Ethylene Oxide |
| Catheter Length (In.) | 35 |
| Product Brand | ON-Q* |
| Kit, Pack, or Tray | True |
Avanos Medical ON-Q Pain Relief System with Dual SILVERSOAKER Antimicrobial Catheters PM045-A Device Characteristics
| 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: | Yes |
| Prescription Use (Rx): | No |
| Over the Counter (OTC): | No |
| Kit: | No |
| Combination Product: | No |
| Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P): | No |
