Identity
- Trade Name
- ARIAL FDA UDI
- Generic Name
- Ambulatory call button FDA UDI
- Device Name
- REFURBISHED - Arial Wireless Water-Resistant Pendant ES with Wristband FDA UDI
- Model / Reference
- 2560-59361R FDA UDI
- Description
- REFURBISHED - Arial Wireless Water-Resistant Pendant ES with Wristband FDA UDI
Identifiers
- Catalog Number
- 1 FDA UDI
- Primary DI / UDI-DI
- 00840948102837 FDA UDI
- FDA Product Code
- IQA FDA UDI
- GMDN Term
- Ambulatory call button FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.3725 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Ambulatory call button
Arial by Securitas Healthcare LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Securitas Healthcare LLC
Sources (1)
- FDA UDI de9eb6df-dc33-4d4a-9713-15610443b212 34 fields · synced May 30, 2026