Catalog Number

vkmc300

Brand Name

Avaline Medical NJ LLC

Version/Model Number

vkmc300

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

KYW

Product Code Name

CONTAINER, LIQUID MEDICATION, GRADUATED

Public Device Record Key

5de3c852-ce8a-44e4-84f2-0222c28d90b9

Public Version Date

March 14, 2022

Public Version Number

1

DI Record Publish Date

March 05, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-