DEVICE: LUMIX C.P.S. (08057949171690)
Device Identifier (DI) Information
LUMIX C.P.S.
LUMIX C.P.S. 5
In Commercial Distribution
LCPS29
FISIOLINE SRL
LUMIX C.P.S. 5
In Commercial Distribution
LCPS29
FISIOLINE SRL
LASER THERAPY UNIT LUMIX C.P.S with 5 WAVELENGTH (650nm+810nm+910nm+980nm+1064nm)
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| Yes | |
| No | |
| Yes | |
| No | |
| No | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 36775 | Skin laser scanner |
An electromechanical device intended to enable a laser beam, produced by an appropriate laser, to be scanned uniformly over a broad field of skin, typically for the removal of skin lesions (e.g., birthmarks, pigmentations) and tattoos. A laser beam is typically so intensely focused that only a tiny area can be treated at a time; large areas of skin must be treated using a scanner which sweeps the beam back and forth over the total target area.
|
Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| ILY | Lamp, Infrared, Therapeutic Heating |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| K160947 | 000 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| No storage/handling found |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Lumen/Inner Diameter: 10 Millimeter |
| Lumen/Inner Diameter: 650 Nanometer |
| Lumen/Inner Diameter: 810 Nanometer |
| Lumen/Inner Diameter: 980 Nanometer |
| Lumen/Inner Diameter: 1064 Nanometer |
| Lumen/Inner Diameter: 910 Nanometer |
Device Record Status
de136717-50e8-461e-8f29-a2d5410d8bfa
June 21, 2023
1
June 13, 2023
June 21, 2023
1
June 13, 2023
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+390172470432
fisioline@fisioline.com
fisioline@fisioline.com