Identity
- Trade Name
- DAAVLIN FDA UDI
- Generic Name
- Ultraviolet phototherapy unit, professional FDA UDI
- Device Name
- 3 Series NeoLux MMCT 311-40 FDA UDI
- Model / Reference
- NEOLUX MMCT FDA UDI
- Description
- 3 Series NeoLux MMCT 311-40 FDA UDI
Identifiers
- Catalog Number
- 864NL0040MMCT FDA UDI
- Primary DI / UDI-DI
- B280864NL0040MMCT07 FDA UDI
- 510(k) Number
- K153749 FDA UDI
- FDA Product Code
- FTC FDA UDI
- GMDN Term
- Ultraviolet phototherapy unit, professional FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4630 FDA UDI
- Commercial Distribution
- Not 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
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
Daavlin by Daavlin Distributing Co., The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Daavlin Distributing Co., The
Sources (1)
- FDA UDI 042f9a6c-d32d-4bbc-a4be-ddb187a4a03c 37 fields · synced Jun 1, 2026