Hailie Sensor - for use only with Flovent HFA

GUDID 09421032180200

Non-rechargeable battery

ADHERIUM (NZ) LIMITED

Inhaler dose sensor

• Primary Device ID: 09421032180200
• NIH Device Record Key: 289914a4-39f9-4814-9d42-b551f3cdfc39
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hailie Sensor - for use only with Flovent HFA
• Version Model Number: NF0091
• Company DUNS: 590654401
• Company Name: ADHERIUM (NZ) 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: false
• Lot Batch: false
• 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: true

Customer Support Contacts

• Phone: 1 (833) 886 9688
• Email: support@hailie.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	09421032180200 [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: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2020-04-27
• Device Publish Date: 2016-09-24

On-Brand Devices [Hailie Sensor - for use only with Flovent HFA]

• 94210321800503: Non-rechargeable battery
• 94210321800398: Rechargeable battery
• 09421032180200: Non-rechargeable battery