Catalog Number

23275-530

Brand Name

V. Mueller

Version/Model Number

23275-530

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

EFQ

Product Code Name

GAUZE/SPONGE, INTERNAL

Public Device Record Key

80c731fe-f576-4aef-9870-c4d6903b4a1f

Public Version Date

March 15, 2021

Public Version Number

3

DI Record Publish Date

September 21, 2016

Package DI Number

50885403067660

Quantity per Package

20

Contains DI Package

70885403067664

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case