FDA UDI In Commercial Distribution 🇺🇸 United States

Genesis Plus

DI: 00816722021205 · Model: Genesis Plus · CUTERA, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Genesis Plus
Primary DI
00816722021205
Version / Model
Genesis Plus
Company Name
CUTERA, INC.
Labeler DUNS
041071643
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2020-02-06
Public Version Status
Update
Public Device Record Key
d215fc54-b1ef-49d7-967d-c6cbc8f0552d

Device Description

Genesis Plus Laser System

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
PDZ Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
47883 Dermatological solid-state laser system

Identifiers

Type ID
Primary 00816722021205

Customer Contacts