Identity
- Trade Name
- HyLight 200 VSS Applicator for US Hybrid System FDA UDI
- Generic Name
- Multi-modality skin surface treatment system FDA UDI
- Device Name
- HyLight 200 VSS Applicator for US Hybrid System FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- HyLight 200 VSS Applicator for US Hybrid System FDA UDI
Identifiers
- Catalog Number
- AACO10032180 FDA UDI
- Primary DI / UDI-DI
- 17290110122147 FDA UDI
- 510(k) Number
- K203441 FDA UDI
- FDA Product Code
- GEX 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
Yes
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
HyLight 200 VSS Applicator for US Hybrid System by Alma Lasers Ltd. — 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
- Alma Lasers Ltd.
Sources (1)
- FDA UDI e47ba232-d0a5-43cf-b5fb-7485a94ab6fa 36 fields · synced Jun 8, 2026