Catalog Number

7462

Brand Name

Vistec

Version/Model Number

7462

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

GDY

Product Code Name

GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE

Public Device Record Key

1ee48729-3143-4a08-961f-334d7323d37f

Public Version Date

August 24, 2021

Public Version Number

3

DI Record Publish Date

June 30, 2018

Package DI Number

20884527017062

Quantity per Package

2000

Contains DI Package

10884527017065

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE