ENDOTRACHEAL TUBE, WIRE REINFORCED, WITH CUFF

GUDID 04544050081801

Endotracheal Tubes are intended for oral intubation and are indicated for use in airway management and other suitable medical application.

FUJI SYSTEMS CORPORATION

Reinforced endotracheal tube, single-use

• Primary Device ID: 04544050081801
• NIH Device Record Key: ca0803c7-8064-405b-b494-4eab3bd037be
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ENDOTRACHEAL TUBE, WIRE REINFORCED, WITH CUFF
• Version Model Number: I.D. 6.5MM (FR.28), 400MM LONG TYPE
• Company DUNS: 715919973
• Company Name: FUJI SYSTEMS CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04544050081801 [Primary]

FDA Product Code

• BTR: Tube, Tracheal (W/Wo Connector)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-09-24

On-Brand Devices [ENDOTRACHEAL TUBE, WIRE REINFORCED, WITH CUFF ]

• 04544050082464: Endotracheal Tubes are intended for oral intubation and are indicated for use in airway manageme
• 04544050081801: Endotracheal Tubes are intended for oral intubation and are indicated for use in airway manageme
• 04544050055789: Endotracheal Tubes are intended for oral intubation and are indicated for use in airway manageme