Identity
- Trade Name
- myBETAapp FDA UDI
- Generic Name
- Medication reminder application software FDA UDI
- Model / Reference
- Mac Thin Client (Desktop) FDA UDI
Identifiers
- Catalog Number
- 84601063 FDA UDI
- Primary DI / UDI-DI
- 05713495000046 FDA UDI
- FDA Product Code
- NXQ FDA UDI
- GMDN Term
- Medication reminder application software FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
myBETAapp by Phillips-Medisize A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Phillips-Medisize A/S
Sources (1)
- FDA UDI 955746d4-117c-40d7-8a25-6feeb0ff43f4 34 fields · synced May 30, 2026