Identity
- Trade Name
- Limelight EUDAMEDFDA UDI
- Generic Name
- Light-energy skin surface treatment system applicator FDA UDI
- Device Name
- xeo+ Family EUDAMEDLimelight IPL Handpiece for xeo+/xeo+ SA FDA UDI
- Model / Reference
- 7003138 EUDAMEDLimelight FDA UDI
- Description
- Limelight IPL Handpiece for xeo+/xeo+ SA FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00816722022813 EUDAMEDFDA UDI
- Basic UDI-DI
- 00816722021800DN EUDAMED
- FDA Product Code
- GEX FDA UDI
- EMDN Code
- Z12011019 MULTI–PLATFORM LASER EUDAMED
- GMDN Term
- Light-energy skin surface treatment system applicator FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4810 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
Limelight by Cutera, Inc. — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 00816722021800DN | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Cutera, Inc.
- EUDAMED SRN
- US-MF-000010456
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (2)
- EUDAMED c8ad4be2-74ff-4c08-9936-2c506f9a6371 61 fields · synced Jun 18, 2026
- FDA UDI f28dc687-629a-45e5-9315-5110e607d0b8 33 fields · synced May 30, 2026