FDA UDI In Commercial Distribution 🇺🇸 United States

VIVACE ULTRA

DI: G055ABMVIVR010 · Model: VERSION 1.0 · Aesthetics Biomedical, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VIVACE ULTRA
Primary DI
G055ABMVIVR010
Version / Model
VERSION 1.0
Catalog Number
ABMVIVR01
Company Name
Aesthetics Biomedical, Inc.
Labeler DUNS
033599752
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-30
Public Version
1
Public Version Date
2023-01-09
Public Version Status
New
Public Device Record Key
ca0b788b-46dd-4017-85eb-5a895acab86d

Device Description

RADIOFREQUENCY APPLICATOR, INTERFACE BETWEEN CART AND MICRONEEDLE CARTRIDGE

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
Yes
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
OUH Skin Resurfacing Rf Applicator
IYO System, Imaging, Pulsed Echo, Ultrasonic

GMDN Terms

Code Name
66285 Intradermal radio-frequency ablation system

Identifiers

Type ID
Primary G055ABMVIVR010

Premarket Submissions

Submission Number Supplement Number
K221574 000