FDA UDI In Commercial Distribution 🇺🇸 United States

COUPLING FLUID

DI: 00850794007071 · Model: VIVCF02 · VIVEVE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
COUPLING FLUID
Primary DI
00850794007071
Version / Model
VIVCF02
Catalog Number
VIVCF02
Company Name
VIVEVE, INC.
Labeler DUNS
025398094
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-03
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
59a95c55-3943-4d4e-8684-04c24d43db1a

Device Description

Viveve Coupling Fluid, 30ml bottle, each

Device Characteristics

Single Use
Yes
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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
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
Package 10850794007078
Primary 00850794007071

Premarket Submissions

Submission Number Supplement Number
K082962 000