Identity
- Trade Name
- Verilux FDA UDI
- Generic Name
- Neurological visible-light phototherapy unit, home-use FDA UDI
- Model / Reference
- VT32WW3 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00768533140043 FDA UDI
- FDA Product Code
- KZF FDA UDI
- GMDN Term
- Neurological visible-light phototherapy unit, home-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6320 FDA UDI
- 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
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Neurological visible-light phototherapy unit, home-use
Verilux by Bear Down Consulting — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Neurological visible-light phototherapy unit, home-use.
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- Verilux — BEAR DOWN CONSULTING · Class I
- Verilux — BEAR DOWN CONSULTING · Class I
- Verilux — BEAR DOWN CONSULTING · Class I
- Verilux — BEAR DOWN CONSULTING · Class I
- Verilux — BEAR DOWN CONSULTING · Class I
- Verilux — BEAR DOWN CONSULTING · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Bear Down Consulting
Sources (1)
- FDA UDI 64bab24e-58c3-4139-9a72-d4c09c82e6df 32 fields · synced Jun 8, 2026