Identity
- Trade Name
- Apilux FDA UDI
- Generic Name
- Multi-modality skin surface treatment system FDA UDI
- Device Name
- Intense Pulsed Ligh (ILP) for Light Hair Removal abd Dark Hair Removal FDA UDI
- Model / Reference
- SmartPur II FDA UDI
- Description
- Intense Pulsed Ligh (ILP) for Light Hair Removal abd Dark Hair Removal FDA UDI
Identifiers
- Catalog Number
- 01-7102 FDA UDI
- Primary DI / UDI-DI
- 00686209171026 FDA UDI
- FDA Product Code
- ONF FDA UDI
- GMDN Term
- Multi-modality skin surface treatment system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Apilux by Dectro International — 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
- Dectro International
Sources (1)
- FDA UDI 967a817f-3ef1-4112-8be7-3f48742faa70 35 fields · synced May 30, 2026