Avanos Medical 7180-20 - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit, 20 FR, PULL, 2/Case
Avanos Medical 7180-20 - MIC Safety Percutaneous Endoscopic Gastrostomy Pull PEG Kit
The MIC Safety PEG Kit - Push Method helps prevent unintentional pullouts of feeding tubes which can reduce emergency room visits, surgical consultations and replacement tubes. This saves thousands of dollars, valuable time, needless patient anguish and life-threatening events. The MIC PEG Feeding Tube design will help eliminate these problems and deliver the security you and your patients expect.The included ventilated SECUR-LOK retention ring allows air circulation around the stoma. Additionally, multiple ports accommodate nutrition and medication delivery. The design also features a radiopaque stripe and bumper aid catheter visualization, as well as a uniquely designed internal retention bumper.
Pull PEG Kit includes:
Traction Removable PUSH PEG Tube Retrieval Snare Feeding Adapter External Retention Bolster 5ml Vial 1% Lidocaine HCl 22ga X 1.5in Safety Needle and 6ml syringe Povidone Iodine Ointmen Fenestrated Drape with Adhesive Tabs Safety Scalpel with #11 Blade | Introducer Safety Needle, 17 ga PullLooped Placement Wire Stainless Steel Scissors Stainless Steel Hemostat Tubing Clamp Water-Soluble Lubricant 4in X 4in Gauze Sponges 2in X 2in Split Gauze Sponges Chloraprep Swabstick Packet Lidocaine Syringe Label |
Avanos Medical 7180-20 - MIC Safety Percutaneous Endoscopic Gastrostomy Pull PEG Kit Features & Benefits
- Medical grade silicone construction
- Ventilated SECUR-LOK retention ring allows air circulation around stoma
- Multiple ports accommodate nutrition and medication delivery
- Radiopaque stripe and bumper aid catheter visualization
- Uniquely designed internal retention bumper
Avanos Medical 7180-20 - MIC Safety Percutaneous Endoscopic Gastrostomy Pull PEG Kit Specifications
| Diameter (Fr) | 20 |
| Product Brand | MIC |
Avanos Medical MIC Safety Percutaneous Endoscopic Gastrostomy Pull PEG Kit 7180-20 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"": | Yes |
| For Single-Use: | Yes |
| Prescription Use (Rx): | No |
| Over the Counter (OTC): | No |
| Kit: | Yes |
| Combination Product: | No |
| Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P): | No |
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