Identity
- Trade Name
- MONITOR,PRO,TABS W/PLASTIC BKT & RESET, CE FDA UDI
- Generic Name
- Vulnerable patient home alert system FDA UDI
- Device Name
- MONITOR,PRO,TABS W/PLASTIC BKT & RESET, CE FDA UDI
- Model / Reference
- 25222CE FDA UDI
- Description
- MONITOR,PRO,TABS W/PLASTIC BKT & RESET, CE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840948101571 FDA UDI
- FDA Product Code
- KMI FDA UDI
- GMDN Term
- Vulnerable patient home alert system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.2400 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
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Monitor, Pro, Tabs W/Plastic Bkt & Reset, Ce by Securitas Healthcare LLC — 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
- Securitas Healthcare LLC
Sources (1)
- FDA UDI 6d8c4b89-60cc-4d3c-94ca-a2579b756253 35 fields · synced May 31, 2026