Reinforced Endotracheal Tube

GUDID 16944932782027

Reinforced Endotracheal tube (Uncuffed)6.5

Well Lead Medical Co.,Ltd

Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use Reinforced endotracheal tube, single-use

• Primary Device ID: 16944932782027
• NIH Device Record Key: 000e6a9a-5a42-49a2-87aa-4123df005ec9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reinforced Endotracheal Tube
• Version Model Number: A01E02653F
• Company DUNS: 544811862
• Company Name: Well Lead Medical Co.,Ltd
• 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: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06944932782020 [Primary]
GS1	16944932782027 [Package]; Contains: 06944932782020; Package: Box [10 Units]; In Commercial Distribution
GS1	26944932782024 [Package]; Package: Carton [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K073383

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-05
• Device Publish Date: 2024-01-27

On-Brand Devices [Reinforced Endotracheal Tube]

• 16944932782089: Reinforced Endotracheal tube (Uncuffed)9.5
• 16944932782072: Reinforced Endotracheal tube (Uncuffed)9.0
• 16944932782065: Reinforced Endotracheal tube (Uncuffed)8.5
• 16944932782058: Reinforced Endotracheal tube (Uncuffed)8.0
• 16944932782041: Reinforced Endotracheal tube (Uncuffed)7.5
• 16944932782034: Reinforced Endotracheal tube (Uncuffed)7.0
• 16944932782027: Reinforced Endotracheal tube (Uncuffed)6.5
• 16944932782003: Reinforced Endotracheal tube (Uncuffed)6.0
• 16944932781990: Reinforced Endotracheal tube (Uncuffed)5.5
• 16944932781983: Reinforced Endotracheal tube (Uncuffed)5.0
• 16944932781976: Reinforced Endotracheal tube (Uncuffed)4.5
• 16944932781969: Reinforced Endotracheal tube (Uncuffed)4.0
• 16944932781952: Reinforced Endotracheal tube (Uncuffed)3.5
• 16944932781945: Reinforced Endotracheal tube (Uncuffed)3.0
• 16944932738734: Reinforced Endotracheal tube (Cuffed)9.5
• 16944932738727: Reinforced Endotracheal tube (Cuffed)9.0
• 16944932738710: Reinforced Endotracheal tube (Cuffed)8.5
• 16944932738703: Reinforced Endotracheal tube (Cuffed)8.0
• 16944932738697: Reinforced Endotracheal tube (Cuffed)7.5
• 16944932738680: Reinforced Endotracheal tube (Cuffed)7.0
• 16944932738673: Reinforced Endotracheal tube (Cuffed)6.5
• 16944932738666: Reinforced Endotracheal tube (Cuffed)6.0
• 16944932738659: Reinforced Endotracheal tube (Cuffed)5.5
• 16944932738642: Reinforced Endotracheal tube (Cuffed)5.0