Catalog Number

S5H01A32-100TC

Brand Name

TRUEplus

Version/Model Number

TRUEplus 3-Bevel Pen Needle 32G/4mm - 100ct box

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

K180720,K180720,K180720

Product Code

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

da1acc52-580e-4a87-b4bb-277d1ba31c78

Public Version Date

March 11, 2019

Public Version Number

1

DI Record Publish Date

February 20, 2019

Package DI Number

10021292012813

Quantity per Package

30

Contains DI Package

00021292012816

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case