Identity
- Trade Name
- Aionex Nurse Call System FDA UDI
- Generic Name
- Nurse call system FDA UDI
- Device Name
- Aionex Nurse Call System provides patients the ability to place a call from their patient location--patient room or other--with full nurse call functionality. The staff are aware of patient calls by visual clues outside the patient room, at a group location such as the nurse station, and/or in a centralized concierge patient response center location designated by the facility. This includes support for routine patient calls as well as emergent patient calls such as Code Blue, Bath Emergency, Bed Exit. Typical locations are clinical care settings. FDA UDI
- Model / Reference
- 1.0 FDA UDI
- Description
- Aionex Nurse Call System provides patients the ability to place a call from their patient location--patient room or other--with full nurse call functionality. The staff are aware of patient calls by visual clues outside the patient room, at a group location such as the nurse station, and/or in a centralized concierge patient response center location designated by the facility. This includes support for routine patient calls as well as emergent patient calls such as Code Blue, Bath Emergency, Bed Exit. Typical locations are clinical care settings. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00852803008000 FDA UDI
- FDA Product Code
- ILQ FDA UDI
- GMDN Term
- Nurse call system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.3710 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Nurse call system
Aionex Nurse Call System by Aionex, Inc. — 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
- Aionex, Inc.
Sources (1)
- FDA UDI 8b68eded-767f-4cca-bb59-be53a2e235d0 34 fields · synced May 30, 2026