Catalog Number

-

Brand Name

Unifine Pentips Plus

Version/Model Number

AN 2840

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

65c19783-9ccf-432a-b7d6-f584505e9b3a

Public Version Date

March 17, 2022

Public Version Number

4

DI Record Publish Date

September 19, 2016

Package DI Number

00384702840028

Quantity per Package

6

Contains DI Package

00384702840011

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Sleeve