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Lumix Plus
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref LPLUS1602HPModel LUMIX C.P.S.Model LUMIX PLUS
Identity
- Trade Name
- LUMIX PLUS EUDAMEDLUMIX ULTRA/PLUS FDA UDI
- Generic Name
- Skin laser scanner FDA UDI
- Device Name
- LASER THERAPY UNIT LUMIX ULTRA/PLUS with 4 WAVELENGTH (650nm+810nm+910nm+980nm) FDA UDI
- Model / Reference
- LUMIX C.P.S. EUDAMEDLPLUS1602HP EUDAMEDLUMIX PLUS EUDAMEDLUMIX ULTRA 3 FDA UDI
- Description
- LASER THERAPY UNIT LUMIX ULTRA/PLUS with 4 WAVELENGTH (650nm+810nm+910nm+980nm) FDA UDI
Identifiers
- Catalog Number
- LPLUS1602HP FDA UDI
- Primary DI / UDI-DI
- 08057949171638 EUDAMEDFDA UDI
- Basic UDI-DI
- 805794917001LAST3U EUDAMEDB-08057949171638 EUDAMED
- Direct Marketing DI
- 08057949171638 EUDAMED
- 510(k) Number
- K161198 FDA UDI
- FDA Product Code
- ILY FDA UDI
- EMDN Code
- Z120615 THERAPEUTIC LASERS EUDAMED
- GMDN Term
- Skin laser scanner FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 890.5500 FDA UDI
- Market of Registration
- Italy 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
No
FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 20 Millimeter FDA UDILumen/Inner Diameter — 980 Nanometer FDA UDILumen/Inner Diameter — 910 Nanometer FDA UDILumen/Inner Diameter — 810 Nanometer FDA UDILumen/Inner Diameter — 650 Nanometer FDA UDI
Lumix Plus by Fisioline Srl — Class IIb — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 805794917001LAST3U | Class IIb | Active |
| EUDAMED | European Union | CE/MDR | 805794917001LAST3U | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Fisioline Srl
- EUDAMED SRN
- IT-MF-000027924
Sources (3)
- EUDAMED 08f895c4-0759-4ad3-ae6a-25f95a12e7ab 61 fields · synced Jun 18, 2026
- EUDAMED fd98b1f8-7149-4656-b925-30b149e42696 61 fields · synced May 19, 2026
- FDA UDI bd935380-e48c-4ffd-bf6e-6e5976349808 38 fields · synced May 30, 2026