Catalog Number

-

Brand Name

DUPLOTIP

Version/Model Number

SA375003000000

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

K033589,K033589

Product Code

FMF

Product Code Name

Syringe, Piston

Public Device Record Key

e5b7ec3e-d8fa-4247-bfcb-c95138e5218a

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 25, 2016

Package DI Number

10815634020136

Quantity per Package

3

Contains DI Package

00815634020139

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

SHELF BOX