myBETAapp 84601063

GUDID 05713495000039

Phillips-Medisize A/S

Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software Medication reminder application software 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)