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Alice NightOne, Non-Wireless Device, INTL
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 1114803
Identity
- Trade Name
- Alice NightOne, Non-Wireless Device, INTL EUDAMEDAlice NightOne FDA UDI
- Generic Name
- Polysomnograph FDA UDI
- Device Name
- Alice NightOne System EUDAMEDAlice NightOne (Non-Wireless), International FDA UDI
- Model / Reference
- 1114803 EUDAMEDAlice NightOne, Non-Wireless Device, INTL FDA UDI
- Description
- Alice NightOne (Non-Wireless), International FDA UDI
Identifiers
- Catalog Number
- 1114803 FDA UDI
- Primary DI / UDI-DI
- 00606959039803 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00606959039803 EUDAMED
- FDA Product Code
- MNR FDA UDI
- EMDN Code
- Z12100501 POLYSOMNOGRAPHS EUDAMED
- GMDN Term
- Polysomnograph FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 868.2375 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Alice NightOne, Non-Wireless Device, INTL by Respironics, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00606959039803 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Respironics Inc.
- EUDAMED SRN
- US-MF-000002301
- Authorised Representative
- Respironics Deutschland GmbH & Co.KG DE-AR-000006164
Sources (3)
- EUDAMED 6a9feb48-81ab-45bf-ac91-8c4a9d40add8 61 fields · synced Aug 1, 2026
- FDA UDI 35433187-821c-4e15-93df-3fc008b9e7a6 36 fields · synced May 30, 2026
- EUDAMED 10314993-0663-4428-a849-dc8b18ae287a 61 fields · synced Aug 1, 2026