Hailie Sensor - for use only with Symbicort MDI

GUDID 94210321800589

Non-rechargeable battery

ADHERIUM (NZ) LIMITED

Inhaler dose sensor

• Primary Device ID: 94210321800589
• NIH Device Record Key: 4893f23b-5717-4f9a-a69b-88cd30ec994c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hailie Sensor - for use only with Symbicort MDI
• Version Model Number: NF0092
• 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
• Phone: 1 (833) 886 9688
• Email: support@hailie.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	94210321800589 [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: 2
• Public Version Date: 2019-06-12
• Device Publish Date: 2018-05-22

On-Brand Devices [Hailie Sensor - for use only with Symbicort MDI]

• 94210321800589: Non-rechargeable battery
• 09421032180422: Inhaler dose sensor
• 09421032180415: Inhaler dose sensor
• 09421032180408: Inhaler dose sensor