Catalog Number

0604170

Brand Name

Port Access Needle

Version/Model Number

0604170

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"

-

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

-

Product Code

FMI

Product Code Name

Needle, hypodermic, single lumen

Public Device Record Key

48024c9f-aa7b-4205-aebe-4dc8f0d1c91d

Public Version Date

October 23, 2019

Public Version Number

3

DI Record Publish Date

September 16, 2016

Package DI Number

10801741037563

Quantity per Package

20

Contains DI Package

00801741037566

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA