FDA UDI In Commercial Distribution 🇺🇸 United States

truSculpt

DI: 00816722021410 · Model: truSculpt 2 MHz · CUTERA, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
truSculpt
Primary DI
00816722021410
Version / Model
truSculpt 2 MHz
Company Name
CUTERA, INC.
Labeler DUNS
041071643
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-21
Public Version
4
Public Version Date
2023-06-08
Public Version Status
Update
Public Device Record Key
b120c23d-5963-4b35-b173-4a899e596e5d

Device Description

truSculpt 3D RF Device

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
GEI Electrosurgical, Cutting & Coagulation & Accessories
PBX Massager, Vacuum, Radio Frequency Induced Heat

GMDN Terms

Code Name
45219 Radio-frequency skin contouring system

Identifiers

Type ID
Primary 00816722021410

Customer Contacts