Catalog Number

76D-4

Brand Name

Integra® Miltex®

Version/Model Number

76D-4

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

-

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

EEF

Product Code Name

CLAMP, RUBBER DAM

Public Device Record Key

fa2493bd-7099-4c83-b398-10722f192efe

Public Version Date

February 05, 2020

Public Version Number

3

DI Record Publish Date

January 22, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-