FDA UDI In Commercial Distribution 🇺🇸 United States

VibrantVue

DI: 00850013056095 · Model: VibrantVue Saline Samples · DRY EYE INNOVATIONS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VibrantVue
Primary DI
00850013056095
Version / Model
VibrantVue Saline Samples
Company Name
DRY EYE INNOVATIONS, LLC
Labeler DUNS
043208431
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-01
Public Version
2
Public Version Date
2026-03-16
Public Version Status
Update
Public Device Record Key
c7e779ee-1961-4a8e-a4d2-c82e4449a819

Device Description

Sterile, preservative-free, unbuffered saline solution in a single dose 5 ml vial.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MRC Products, Contact Lens Care, Rigid Gas Permeable

GMDN Terms

Code Name
60838 Contact lens rinsing solution

Identifiers

Type ID
Primary 00850013056095

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
32 – Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
0 – Degrees Celsius