Catalog Number

-

Brand Name

Pentips

Version/Model Number

AN 3429

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K152339,K152339,K152339,K152339

Product Code

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

0bed7030-d004-4dae-8e41-727b58b9f852

Public Version Date

October 14, 2021

Public Version Number

4

DI Record Publish Date

September 19, 2016

Package DI Number

00384703429031

Quantity per Package

50

Contains DI Package

00384703429024

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case