Catalog Number

03190

Brand Name

Curity

Version/Model Number

03190

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

FRL

Product Code Name

FIBER, MEDICAL, ABSORBENT

Public Device Record Key

83839522-b224-49d8-bc24-5640a8dd7118

Public Version Date

August 07, 2020

Public Version Number

3

DI Record Publish Date

June 22, 2018

Package DI Number

10884521121744

Quantity per Package

1000

Contains DI Package

10884521209305

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE