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VibrantVue

FDA UDI

Class U (US FDA UDI)

by Dry Eye Innovations, Llc

Identity

Trade Name
VibrantVue FDA UDI
Generic Name
Antimicrobial wound irrigation solution FDA UDI
Device Name
Hand Cleanser 2oz FDA UDI
Model / Reference
2020.03 FDA UDI
Description
Hand Cleanser 2oz FDA UDI

Identifiers

Catalog Number
1HC2 FDA UDI
Primary DI / UDI-DI
00850013056057 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Antimicrobial wound irrigation solution FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 2 Fluid Ounce FDA UDI

Category: Antimicrobial wound irrigation solution

VibrantVue by Dry Eye Innovations, Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antimicrobial wound irrigation solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e222448-1599-4278-b58c-e3a2440ef703 37 fields · synced May 30, 2026