FDA UDI Not in Commercial Distribution 🇺🇸 United States

VelaShape III system

DI: 07290109952031 · Model: FG71201 · SYNERON MEDICAL LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VelaShape III system
Primary DI
07290109952031
Version / Model
FG71201
Catalog Number
FG71201
Company Name
SYNERON MEDICAL LTD
Labeler DUNS
532685716
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-25
Public Version
6
Public Version Date
2023-10-17
Public Version Status
Update
Public Device Record Key
be476f83-2a6e-47aa-a192-6e77a18aee5d
Distribution End Date
2023-10-16

Device Description

VelaShape III System 120V, Packaged

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
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

GMDN Terms

Code Name
44832 Multi-modality skin contouring system

Identifiers

Type ID
Primary 07290109952031

Premarket Submissions

Submission Number Supplement Number
K122579 000