Catalog Number

23275-670

Brand Name

V. Mueller

Version/Model Number

23275-670

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GDY

Product Code Name

GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE

Public Device Record Key

d521e9d7-cc76-4302-a7b0-e64aeeee8f45

Public Version Date

August 13, 2018

Public Version Number

1

DI Record Publish Date

July 12, 2018

Package DI Number

50885403067769

Quantity per Package

50

Contains DI Package

70885403067763

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case