FDA UDI In Commercial Distribution 🇺🇸 United States

LUSTER Handpiece

DI: 07290117772409 · Model: NA · LUMENIS BE LTD
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUSTER Handpiece
Primary DI
07290117772409
Version / Model
NA
Company Name
LUMENIS BE LTD
Labeler DUNS
600763501
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-22
Public Version
1
Public Version Date
2024-01-30
Public Version Status
New
Public Device Record Key
1ed5be68-91e5-44b8-b2b7-4c31f0ee9f56

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument
ONG Powered Laser Surgical Instrument With Microbeam\Fractional Output

GMDN Terms

Code Name
47883 Dermatological solid-state laser system

Identifiers

Type ID
Primary 07290117772409

Premarket Submissions

Submission Number Supplement Number
K222790 000