Catalog Number

6474

Brand Name

Curity

Version/Model Number

6474

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

7ddeadaf-d3a9-4abe-9705-f64c65443e44

Public Version Date

February 15, 2019

Public Version Number

3

DI Record Publish Date

June 28, 2018

Package DI Number

20884521087368

Quantity per Package

10

Contains DI Package

10884521087361

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE