Home GUDID 16944932784083
Endotracheal Tube with Evacuation Lumen
Primary DI 16944932784083
Brand Endotracheal Tube with Evacuation Lumen
Company Well Lead Medical Co.,Ltd
Model A01G04754F
Device description PU Cuff 7.5 DEHP FREE
Published 2024-01-27
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name BTR Tube, Tracheal (W/Wo Connector)
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class BTR Tube, Tracheal (W/Wo Connector) Anesthesiology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 16944932784083 Package GS1 10 In Commercial Distribution 26944932784080 Package GS1 10 In Commercial Distribution 06944932784086 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 16944932784083 16944932784083 26944932784080 26944932784080 06944932784086 06944932784086 6944932784086
GMDN Terms# Term, Definition table Term Definition Basic endotracheal tube, single-use A hollow cylinder inserted orally or nasally into the trachea to provide an unobstructed airway to convey gases and vapours to and from the lungs during anaesthesia, resuscitation, and other situations where the patient is not properly ventilated; it does not include an antimicrobial agent(s). The device may: 1) be packaged with a connector that will attach to a breathing circuit or manual resuscitator; 2) have a distal inflatable cuff to seal against the tracheal wall; 3) be radiopaque; and 4) have a built-in pilot balloon for cuff pressure monitoring. It is available in various diameters and lengths for adult and paediatric patients. This is a single-use device.
Regulatory Flags# DUNS number 544811862 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 06925816656057 Suction Catheter FN02A060620 2026-06-03 06925816673962 Wellead Hydrophilic Intermittent Catheter F01L030830 2026-04-03 06925816673979 Wellead Hydrophilic Intermittent Catheter F01L031030 2026-04-03 06925816673986 Wellead Hydrophilic Intermittent Catheter F01L031230 2026-04-03 06925816673993 Wellead Hydrophilic Intermittent Catheter F01L031430 2026-04-03 06925816674006 Wellead Hydrophilic Intermittent Catheter F01L031630 2026-04-03 06925816674013 Wellead Hydrophilic Intermittent Catheter F01L031830 2026-04-03 06925816674020 Wellead Hydrophilic Intermittent Catheter F01L020820 2026-04-03 06925816674037 Wellead Hydrophilic Intermittent Catheter F01L021020 2026-04-03 06925816674044 Wellead Hydrophilic Intermittent Catheter F01L021220 2026-04-03 06925816674051 Wellead Hydrophilic Intermittent Catheter F01L021420 2026-04-03 06925816674068 Wellead Hydrophilic Intermittent Catheter F01L021620 2026-04-03 06925816674075 Wellead Hydrophilic Intermittent Catheter F01L021820 2026-04-03 06925816674082 Wellead Hydrophilic Intermittent Catheter F01L041030 2026-04-03 06925816674099 Wellead Hydrophilic Intermittent Catheter F01L041230 2026-04-03 06925816674105 Wellead Hydrophilic Intermittent Catheter F01L041430 2026-04-03 06925816674112 Wellead Hydrophilic Intermittent Catheter F01L041630 2026-04-03 06925816674129 Wellead Hydrophilic Intermittent Catheter F01L041830 2026-04-03 06925816674136 Wellead Hydrophilic Intermittent Catheter F01L010810 2026-04-03 06925816674143 Wellead Hydrophilic Intermittent Catheter F01L011010 2026-04-03
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