Mouthpiece

GUDID 06934325303741

FEELLIFE HEALTH INC.

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• Primary Device ID: 06934325303741
• NIH Device Record Key: 12dbbcfd-2ff1-40fe-8423-9ef621341dda
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mouthpiece
• Version Model Number: MP1
• Company DUNS: 544431678
• Company Name: FEELLIFE HEALTH INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06934325303741 [Primary]

FDA Product Code

• BYP: Mouthpiece, Breathing

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: 2023-02-22
• Device Publish Date: 2023-02-14

Devices Manufactured by FEELLIFE HEALTH INC.

• 06934325302294 - Spirometer: 2023-09-27
• 06934325303741 - Mouthpiece: 2023-02-22
• 06934325303741 - Mouthpiece: 2023-02-22
• 06934325303758 - Disposable Mouthpiece: 2023-02-22
• 06934325303765 - Pressure gas blowpipe: 2023-02-22
• 06934325302249 - Portable Mesh Nebulizer: 2023-02-16
• 06934325302263 - Portable Mesh Nebulizer: 2023-02-16
• 06934325301846 - Portable Mesh Nebulizer: 2022-10-17
• 06934325319490 - Portable Mesh Nebulizer: 2021-08-27