FDA UDI In Commercial Distribution 🇺🇸 United States

VIVEVE Footswitch

DI: 00850794007170 · Model: VIVFS01 · VIVEVE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VIVEVE Footswitch
Primary DI
00850794007170
Version / Model
VIVFS01
Catalog Number
VIVFS01
Company Name
VIVEVE, INC.
Labeler DUNS
025398094
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
48eeffbd-8ba8-4f55-8530-3afa6d7d665b

Device Description

Viveve Footswitch

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
No
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
45219 Radio-frequency skin contouring system

Identifiers

Type ID
Primary 00850794007170

Premarket Submissions

Submission Number Supplement Number
K082962 000