Product Description
Avanos Medical 2401253-5 - BALLARD* Multi-Access Port Closed Suction Replacement Catheter, 12 Fr, 13.8 IN Catheter Length, 20/CS
Avanos Medical 2401253-5 - Ballard Multi-Access Port Closed Suction Replacement Catheter
The BALLARD* Multi-Access Port (MAP) Closed Suction System features a compact rotating manifold that provides multiple ports to access the patients airway without jeopardizing integrity of the closed circuit. A closed circuit helps you protect your patient from cross-contamination and VAP. Clinicians can perform suctioning and other procedures such as bronchoalveolar lavage, bronchoscopy, or MDI drug delivery while maintaining a closed vent circuit as recommended to help prevent VAP.
Avanos Medical 2401253-5 - Ballard Multi-Access Port Closed Suction Replacement Catheter Features & Benefits
- Replacement catheter for Multi-Access Port (MAP) catheter system
- Includes BALLARD* Turbo-Cleaning chamber for a cleaner catheter
- Sleeve tether prevents over-retraction of catheter
- Depth markings for easy and proper depth suctioning
- Soft low durometer catheter to minimize tracheal trauma
- Tactile sleeve for catheter advancement
- BALLARD* Technology
- Built-in Cleaning Chamber
- Gamma Sterilised: 3 Years Shelf Life
- Tethered Sleeve
- Tethered Cap
- Available for Endotracheal and Tracheostomy Tubes
- Suction Catheter: Validated for a maximum Usage Time of 72 Hours
- Does not contain Natural Rubber Latex nor DEHP
Avanos Medical 2401253-5 - Ballard Multi-Access Port Closed Suction Replacement Catheter Specifications
| Diameter (Fr) | 12 |
| Made With DEHP | No |
| Single Use | True |
| Sterile | Yes |
| Sterilization Method | GAMMA |
| Catheter Length (In.) | 13.8 |
| MDI Attachment | No |
| Primary Product Color | White |
| Product Brand | BALLARD |
| Kit, Pack, or Tray | False |
Avanos Medical Ballard Multi-Access Port Closed Suction Replacement Catheter 2401253-5 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 |
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