HME-Booster T-Piece

GUDID 05055788792277

FLEXICARE MEDICAL LIMITED

Tube/mask breathing circuit connector, single-use, non-sterile

• Primary Device ID: 05055788792277
• NIH Device Record Key: 107f2a7c-f60e-4ad5-8276-c6522b9391a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HME-Booster T-Piece
• Version Model Number: 360-000-000U
• Company DUNS: 504406273
• Company Name: FLEXICARE MEDICAL LIMITED
• 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: false
• Expiration Date: true
• Donation Id Number: false
• 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	05055788792277 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122885

FDA Product Code

• BTT: Humidifier, Respiratory Gas, (Direct Patient Interface)

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: 2019-04-16
• Device Publish Date: 2019-04-08

On-Brand Devices [HME-Booster T-Piece]

• 05055788792277: 360-000-000U
• 05055788778554: 360-000-000