Catalog Number

-

Brand Name

NETCELL

Version/Model Number

30-380

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 28, 2022

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

KCN

Product Code Name

Ear Wick

Public Device Record Key

5d913161-efc4-4be8-b14a-024d320394dd

Public Version Date

July 29, 2022

Public Version Number

2

DI Record Publish Date

August 06, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-