SootheNeb

GUDID 00816042014659

Compressor Nebulizer

FORA CARE INC.

Benchtop nebulizer, non-heated

• Primary Device ID: 00816042014659
• NIH Device Record Key: 08689ce3-08a9-49fb-825e-80c74c0823b8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SootheNeb
• Version Model Number: NBL300g
• Company DUNS: 004340807
• Company Name: FORA CARE INC.
• 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: true
• Manufacturing Date: true
• Expiration Date: false
• 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	00816042014659 [Primary]

FDA Product Code

• CAF: Nebulizer (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: 2023-07-10
• Device Publish Date: 2023-06-30

On-Brand Devices [SootheNeb]

• 00816042012860: Mouthpiece
• 00816042011474: Medication Cup
• 00816042011467: Mesh Cap
• 00816042011153: Compressor Nebulizer
• 00816042011146: Mesh Nebulizer
• 00816042014659: Compressor Nebulizer
• 00816042014758: Compressor Nebulizer