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Alice PDx Sleep Diagnostic System, INTL
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 1043844
Identity
- Trade Name
- Alice PDx Sleep Diagnostic System, INTL EUDAMEDAlice PDx FDA UDI
- Generic Name
- Polysomnograph FDA UDI
- Device Name
- Alice PDx System EUDAMEDAlice PDx Portable Sleep Diagnostics System, International FDA UDI
- Model / Reference
- 1043844 EUDAMEDAlice PDx Sleep Diagnostic System, INTL FDA UDI
- Description
- Alice PDx Portable Sleep Diagnostics System, International FDA UDI
Identifiers
- Catalog Number
- 1043844 FDA UDI
- Primary DI / UDI-DI
- 00606959020481 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00606959020481 EUDAMED
- 510(k) Number
- K090484 FDA UDI
- 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 PDx Sleep Diagnostic System, 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-00606959020481 | 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 3e361b8b-e4c3-46ab-9adf-767c02f737a9 61 fields · synced Jun 19, 2026
- FDA UDI a2d80817-f5ed-45e4-b344-a12838993e05 37 fields · synced May 30, 2026
- EUDAMED 7cf64eab-ea90-4fae-942f-510afc4297ee 61 fields · synced Jun 19, 2026