Catalog Number

-

Brand Name

Integra®

Version/Model Number

3805411

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

Yes

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

-

FDA Premarket Submission

K960248,K960248

Product Code

FMF

Product Code Name

Syringe, piston

Public Device Record Key

8d8b436e-a59c-43af-b512-9154c728b12b

Public Version Date

March 04, 2019

Public Version Number

1

DI Record Publish Date

February 01, 2019

Package DI Number

30381780511322

Quantity per Package

10

Contains DI Package

10381780511328

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case