Identity
- Trade Name
- Conair FDA UDI
- Generic Name
- Home-use hair-removal electrolysis system FDA UDI
- Device Name
- IPL Depilator FDA UDI
- Model / Reference
- IPL 960F FDA UDI
- Description
- IPL Depilator FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00074108368751 FDA UDI
- 510(k) Number
- K172791 FDA UDI
- FDA Product Code
- OHT FDA UDI
- GMDN Term
- Home-use hair-removal electrolysis system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Safe FDA UDI
Category: Home-use hair-removal electrolysis system
Conair by Conair Llc. — 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
- Conair Llc.
Sources (1)
- FDA UDI fa8014df-5c24-437e-8722-5716ab4c5f00 34 fields · synced May 30, 2026