Identity
- Trade Name
- ETERNAL SUN XP*R 9K90 / 180-250W FDA UDI
- Generic Name
- Ultraviolet tanning device FDA UDI
- Model / Reference
- FR79 T12 180W VHO PH / BiPin FDA UDI
Identifiers
- Catalog Number
- 16259 FDA UDI
- Primary DI / UDI-DI
- 04014501000694 FDA UDI
- FDA Product Code
- LEJ FDA UDI
- GMDN Term
- Ultraviolet tanning device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4635 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
No
FDA UDI
Over-the-Counter
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Eternal Sun Xp*r 9k90 / 180-250w by NARVA Lichtquellen GmbH + Co KG. — 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 |
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Manufacturer
- Manufacturer
- NARVA Lichtquellen GmbH + Co KG.
Sources (1)
- FDA UDI 875c87a2-28ab-4cfb-a353-b7fd07b5381a 36 fields · synced Jun 8, 2026