Catalog Number

310030

Brand Name

RITMED ALL GAUZE

Version/Model Number

310030

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"

Yes

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

NAC

Product Code Name

Dressing, wound, hydrophilic

Public Device Record Key

f8a80685-f032-431e-a757-ca9164fbc83f

Public Version Date

June 02, 2020

Public Version Number

1

DI Record Publish Date

May 25, 2020

Package DI Number

20686864056458

Quantity per Package

10

Contains DI Package

10686864056451

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

OUTER CASE