LMA

Basic Information

• Brand Name: LMA
• Primary DI: 05060112313288
• Version / Model: IPN046009
• Catalog Number: EID100
• Company Name: TELEFLEX INCORPORATED
• Labeler DUNS: 002348191
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2016-09-16
• Public Version: 3
• Public Version Date: 2018-07-06
• Public Version Status: Update
• Public Device Record Key: ba5d61ea-4946-4197-b2c9-8df473ff61ac

Device Description

Esophageal Intubation Detector - Syringe

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: Yes
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
BTR	Tube, tracheal (w/wo connector)	Anesthesiology	868.5730	2

GMDN Terms

Code	Name	Definition	Implantable	Status
36290	Suction oesophageal intubation detector, adult	A device designed to verify endotracheal (ET) tube placement by the application of a partial vacuum (using a plunger syringe or a self-inflating bulb) through a small calibre tube introduced into the tracheal tube during airway management. It is used during adult intubation. This device exploits the anatomic difference between the trachea and the oesophagus: when the detector bulb or syringe is depressed (a partial vacuum is applied) it refills with air if the intubation is tracheal, and fails to fill if the intubation is oesophageal (the oesophagus collapses around the tube). It is used in healthcare facilities or in the field to evaluate oesophageal intubation. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	25060112313282	GS1	Case	20	In Commercial Distribution
Primary	05060112313288	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]

Premarket Submissions

Submission Number	Supplement Number
K990556	000