Identity
- Trade Name
- SOMNOscreen HD EEG 32 Set FDA UDI
- Generic Name
- Polysomnograph FDA UDI
- Model / Reference
- NGA300U FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04250413410361 FDA UDI
- GMDN Term
- Polysomnograph FDA UDI
Classification
- 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
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: PolysomnographPatient monitoring system module, multifunction
SOMNOscreen HD EEG 32 Set by Somnomedics GmbH — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Somnomedics GmbH
Sources (1)
- FDA UDI 3e63edfe-cfee-40a4-a7a3-77015149ec6e 32 fields · synced May 31, 2026