myBETAapp 84601063

GUDID 05713495000039

Phillips-Medisize A/S

Medication reminder application software

• Primary Device ID: 05713495000039
• NIH Device Record Key: ddd2f8c1-3b16-4f26-b1ef-0b9541e2f4f0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: myBETAapp
• Version Model Number: Windows Thin Client (Desktop)
• Catalog Number: 84601063
• Company DUNS: 306047440
• Company Name: Phillips-Medisize A/S
• 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: true
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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	05713495000039 [Primary]

FDA Product Code

• NXQ: Reminder, Medication

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: 2021-10-15
• Device Publish Date: 2019-10-07

On-Brand Devices [myBETAapp]

• 05713495000060: Android (Mobile App)
• 05713495000053: iOS (Mobile App)
• 05713495000046: Mac Thin Client (Desktop)
• 05713495000039: Windows Thin Client (Desktop)