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Lcps902

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref LCPS902Model LUMIX CPSModel LUMIX C.P.S.

by Fisioline Srl

Identity

Trade Name
LUMIX C.P.S. EUDAMEDFDA UDI
Generic Name
Skin laser scanner FDA UDI
Device Name
LASER THERAPY UNIT LUMIX C.P.S. with 3 WAVELENGTH (650nm+910nm+1064nm) FDA UDI
Model / Reference
LUMIX CPS EUDAMED
LCPS902 EUDAMED
LUMIX C.P.S. EUDAMED
LUMIX C.P.S.3 FDA UDI
Description
LASER THERAPY UNIT LUMIX C.P.S. with 3 WAVELENGTH (650nm+910nm+1064nm) FDA UDI

Identifiers

Catalog Number
LCPS902 FDA UDI
Primary DI / UDI-DI
08057949170112 EUDAMEDFDA UDI
Basic UDI-DI
B-08057949170112 EUDAMED
805794917001LAST3U EUDAMED
Direct Marketing DI
08057949170112 EUDAMED
510(k) Number
K160947 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 EUDAMED
Class 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 — 1064 Nanometer FDA UDI
Lumen/Inner Diameter — 910 Nanometer FDA UDI
Lumen/Inner Diameter — 650 Nanometer FDA UDI
Lumen/Inner Diameter — 10 Millimeter FDA UDI

Lcps902 by Fisioline Srl — Class IIb — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fisioline Srl
EUDAMED SRN
IT-MF-000027924

Sources (3)

  • EUDAMED 7e38a2d5-45e9-48ff-b52d-b9018b40604d 61 fields · synced Jul 19, 2026
  • EUDAMED c3edcd4f-564d-4b6f-a64e-91d540eac149 61 fields · synced May 18, 2026
  • FDA UDI b902f705-eea8-47bf-9273-72f1e99051f4 38 fields · synced May 30, 2026