Cook Medical G32193 - Set Emergency Cricothyrotomy Universal Ea
Melker Universal Emergency Cricothyrotomy Catheter set
Used for emergency airway access when conventional endotracheal intubation cannot be performed.
The Melker Universal Cricothyrotomy Catheter Tray features devices for both surgical and Seldinger techniques that place freedom of choice and control into the clinicians hands. Designed to establish emergency airway access via the cricothyroid membrane for cannot intubate, cannot ventilate situations.
| Order Number | Reference Part Number | Catheter Length (cm) | Catheter ID (mm) |
| G32193 | C-TCCSB-500-UNI | 9 | 5 |
Features & Benefits
- Airway access is achieved by percutaneous entry (Seldinger) or surgical technique via the cricothyroid membrane.
- Airway access is achieved by either standard wire-guided (Seldinger) or surgical technique via the cricothyroid membrane. Tray contains necessary components for either technique.
- Catheter is cuffed to protect and control the airway once placed.
- Supplied sterile in peel-open packages.
- Intended for one time use.
Components
Surgical Technique & Seldinger Technique
- Introducer needle
- FEP catheter introducer needle
- Syringe
- Scalpel
- Wire guide
- Curved dilator
- Airway catheter
- #11 safety scalpel
- Trousseau dilators
- Tracheal hook
- Blunt, curved dilator
- Trach tape
#1 Surgical TechniqueThis method incorporates a soft, blunted dilator with the Melker Cuffed Cricothyrotomy catheter, following the creation of the tracheal stoma. | #2 Seldinger TechniqueUtilizes an entry needle, wire guide and dilator for a percutaneous insertion of the airway catheter. |
Safety Scalpel
Creates a precise incision for creation of stoma. Safety feature may help protect physician from accidental sticks.
Tracheal Hook
Grasps and elevates the cricothyroid cartilage, allowing more control during airway placement.
Trousseau Dilator
Dilates by spreading stoma.
Curved Blunt Dilator
Blunt-tipped dilator prevents snagging at stoma site and posterior tracheal wall damage.
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): | Yes |
| Over the Counter (OTC): | No |
| Kit: | No |
| Combination Product: | No |
| Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P): | No |
