Posey Cufflators Endotracheal Tube Inflator and Manometer

GUDID 10862229000202

POSEY CUFFLATOR

POSEY PRODUCTS, LLC

Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder Endotracheal tube holder

• Primary Device ID: 10862229000202
• NIH Device Record Key: c7e62a9d-facb-423a-819a-33185aa03e7c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Posey Cufflators Endotracheal Tube Inflator and Manometer
• Version Model Number: 8199
• Company DUNS: 008503294
• Company Name: POSEY PRODUCTS, LLC
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	10862229000202 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K912723

FDA Product Code

• BSK: Cuff, Tracheal Tube, Inflatable

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2022-10-20
• Device Publish Date: 2015-10-31

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