3M Littmann Classic III Monitoring Stethoscope (5807) - Rainbow Finish Chestpiece Caribbean Blue Tube

The 3M Littmann Classic III Monitoring Stethoscope (5807) is engineered for comprehensive physical assessment, patient monitoring, and diagnosis across a diverse patient population, including children and adults. This instrument is suitable for use in non-critical care environments such as medical offices, general wards, OB/GYN, ambulatory clinics, and urgent care settings.

Featuring high acoustic sensitivity, the Littmann Classic III Stethoscope incorporates tunable diaphragm technology, a 3M innovation that allows clinicians to discern both low and high-frequency sounds by simply adjusting pressure on the chestpiece, eliminating the need for repositioning. The dual-sided chestpiece is designed for versatility, accommodating both adult and pediatric patients. The pediatric side can be converted into a traditional open bell by replacing the single-piece diaphragm with a non-chill rim.

Constructed with next-generation tubing, this stethoscope offers enhanced resistance to skin oils and alcohol, contributing to a longer product life and reduced staining. The tubing is manufactured without natural rubber latex or phthalate plasticizers, providing a safer experience for both medical professionals and patients. Snap-tight, soft-sealing eartips ensure an excellent acoustic seal and comfortable fit, while a non-chill diaphragm enhances patient comfort during examinations.

Key Features : 

Facilitates auscultation of heart, lung, and other body sounds for physical assessment, patient monitoring, and diagnosis.
Offers high acoustic sensitivity for exceptional performance in detecting subtle sounds.
Utilizes tunable diaphragm technology for seamless transition between low and high-frequency sound detection.
Features a versatile dual-sided chestpiece suitable for both adult and pediatric patients.
Equipped with next-generation tubing that is free from natural rubber latex and phthalate plasticizers.
Designed with a lightweight profile for enhanced user comfort during extended use.
Complies with the Medical Device Regulation (EU) 2017/745 as a CE marked Class I device.
Listed in the FDA GUDID database, indicating commercial distribution in the United States.