Identity
- Trade Name
- Nox C1 Access Point EUDAMEDFDA UDI
- Generic Name
- Polysomnograph FDA UDI
- Device Name
- Nox C1 Access Point EUDAMED
- Model / Reference
- NOX-SCOM1 EUDAMEDFDA UDINOX-SCOM1US FDA UDI
Identifiers
- Catalog Number
- NA FDA UDI
- Primary DI / UDI-DI
- 15694311110590 EUDAMEDFDA UDI15694311111498 FDA UDI
- Basic UDI-DI
- B-15694311110590 EUDAMED
- 510(k) Number
- K192469 FDA UDI
- FDA Product Code
- OLZ FDA UDIKZM FDA UDI
- EMDN Code
- Z12100501 POLYSOMNOGRAPHS EUDAMED
- GMDN Term
- Polysomnograph FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 882.1400 FDA UDI890.1375 FDA UDI
- Market of Registration
- Iceland 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
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Polysomnograph
Nox C1 Access Point by Nox Medical ehf. — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Cleared under the same submission
K192469 also covers:
- Nox A1 Carry Case — Nox Medical ehf.
- Nox A1 Recorder — Nox Medical ehf.
- Nox A1 Starter Sensor Kit, Adult — Nox Medical ehf.
- Nox A1 Starter Sensor Kit, Pediatric — Nox Medical ehf.
- Nox A1 System — Nox Medical ehf.
- Nox A1s Recorder — Nox Medical ehf.
- Nox A1® EEG 5 Lead Gold Electrode Cable — Nox Medical ehf.
- Nox A1® EEG Head Cable — Nox Medical ehf.
- Nox C1 Kit — Nox Medical ehf.
- Nox C1 Kit — Nox Medical ehf.
- Nox C1s Kit — Nox Medical ehf.
- Noxturnal PSG CD — Nox Medical ehf.
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Nox Medical ehf.
Sources (3)
- FDA UDI a45ee3fa-2a5c-4db7-ac6b-ca81943741fb 34 fields · synced Jul 22, 2026
- FDA UDI c27b010f-6fc2-482d-bec5-6b4b4623a7a8 35 fields · synced May 30, 2026
- EUDAMED b5edc022-6400-4e4c-9d54-e5a7a6dee15a 61 fields · synced Jul 22, 2026