Catalog Number

2146

Brand Name

Curity

Version/Model Number

2146

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NAB

Product Code Name

Gauze / sponge,nonresorbable for external use

Public Device Record Key

fbd6c536-1f34-4157-964f-fd8630f93dd4

Public Version Date

August 24, 2021

Public Version Number

3

DI Record Publish Date

June 22, 2018

Package DI Number

20884521084220

Quantity per Package

5000

Contains DI Package

10884521084223

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE