LMA Protector teliflex

LMA Protector teliflex Specification

Features
Soft seal cuff, easy insertion, cuff indicator, integrated bite block

Shelf Life
5 years

Storage Instructions
Store in a cool, dry place; avoid direct sunlight

Function
Maintain open airway and prevent aspiration

Usage Type
Single-use/Disposable

Instruments Type
Airway device

Equipment Type
Laryngeal Mask Airway

Material
Medical grade silicone

Condition
New

Technology
Teliflex integrated design

Portable
Yes

Wall Mounted
No

Real-Time Operation
Yes

Noise Level
Silent operation

Operating Type
Manual

Use
Airway management during anesthesia

Power Source
None (manual)

Dimension (L*W*H)
Varies by size (sizes available: 3, 4, 5)

Weight
Approx. 60g to 100g based on size

Color
Translucent with color-coded cuff

About LMA Protector teliflex

The LMA Protector Airway is the most advanced second generation airway from Teleflex.

Dual gastric channels

The only laryngeal mask that combines a pharyngeal chamber and dual gastric drainage channels, designed specifically to channel gastric content away from the airway.

Silicone

The airway tube and cuff are 100% silicone, phthalate free and designed to conform to the anatomy. Silicone cuffs have been shown to reduce risk of sore throat1 and achieve higher seal pressures2 compared with PVC cuffs.

Cuff Pilot Technology

An integrated cuff pressure indicator for single-use airway management devices that enables continuous cuff pressure monitoring at a glance and facilitates easy, accurate adjustment when necessary.3,4

Second Seal Technology

The elongated cuff facilitates the upper esophageal seal.

Ability to intubate

Allows direct intubation using visual guidance.

Enhanced Airway Security and Comfort

With its anatomically designed, high-volume, low-pressure cuff, the LMA Protector Teliflex offers a gentle yet reliable seal, reducing the risk of aspiration and airway injury. Its integrated bite block adds protection, making it ideal for both routine anesthesia in the operating room and emergency airway management.

User-Friendly Features for Precision and Safety

The tube's flexibility and resistance to kinking support unimpeded airflow, while depth and size indicator markings aid proper placement. The standard 15 mm connector ensures compatibility with anesthesia circuits. Each device is latex-free, individually sealed, and sterilized for safe single-use operation.

FAQ's of LMA Protector teliflex:

Q: How is the LMA Protector Teliflex used during anesthesia or emergency airway management?

A: This device is inserted to maintain a patent airway and prevent aspiration during procedures requiring anesthesia or when there is a need for rapid airway management. Its anatomically shaped cuff facilitates easy and secure insertion.

Q: What benefits does the integrated bite block provide?

A: The integrated bite block protects the airway tube from occlusion if the patient bites down, safeguarding both the device and the patient's airway during use.

Q: When should the LMA Protector Teliflex be used?

A: It is suitable for adult patients in operating rooms, anesthesia procedures, and emergency airway management situations where a secure, non-invasive airway is needed.

Q: Where can this equipment be utilized?

A: The device is designed for use in hospitals, clinics, and emergency response settings by healthcare professionals experienced in airway management.

Q: What is the sterilization process for the LMA Protector Teliflex?

A: Each device is sterilized using ethylene oxide, ensuring it is ready for immediate single-use upon opening the sterile, individually sealed packaging.

Q: How does the device's design improve clinical application and usability?

A: Its flexible, reinforced tube resists kinking, while depth and size markings help ensure accurate placement. The color-coded cuff and translucent tubing facilitate easy identification and monitoring.

Q: What are the storage and shelf life recommendations for this airway device?

A: Store the LMA Protector Teliflex in a cool, dry environment away from direct sunlight. The device maintains sterility and optimal performance for up to five years from the date of manufacture.