Identity
- Trade Name
- Messenger FDA UDI
- Generic Name
- Alarm application software FDA UDI
- Device Name
- Messenger 5.18.2 Software Release FDA UDI
- Model / Reference
- 5.18.2 FDA UDI
- Description
- Messenger 5.18.2 Software Release FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860011811916 FDA UDI
- FDA Product Code
- MSX FDA UDI
- GMDN Term
- Alarm application software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2300 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Alarm application software
Messenger by Spok Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Alarm application software.
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- Engage Medical Device Alarm Notification System (EMDAN) — Stryker Corp. · Class II
- Engage Medical Device Alarm Notification System (EMDAN) — Stryker Corp. · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Spok Inc.
Sources (1)
- FDA UDI 13f08d83-1189-4e90-9848-072d54368a58 34 fields · synced May 30, 2026