CuffTrek

GUDID 36979264200004

SHANGHAI LONGMANN TECH CO.,LTD.

Endotracheal tube cuff inflator

• Primary Device ID: 36979264200004
• NIH Device Record Key: b1a642e8-4764-4750-9ef7-a2ff0364c08d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CuffTrek
• Version Model Number: LG-1
• Company DUNS: 530703915
• Company Name: SHANGHAI LONGMANN TECH 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: true
• 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	36979264200004 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K242642

FDA Product Code

• BSK: Cuff, Tracheal Tube, Inflatable

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-02-02
• Device Publish Date: 2026-01-23