Catalog Number

-

Brand Name

Hypodermic Needle

Version/Model Number

6972

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K112057,K112057,K112057

Product Code

FMI

Product Code Name

Needle, Hypodermic, Single Lumen

Public Device Record Key

1c8abb2b-b0b6-4450-961f-1242e27434f3

Public Version Date

October 23, 2019

Public Version Number

5

DI Record Publish Date

September 24, 2016

Package DI Number

00616784697239

Quantity per Package

10

Contains DI Package

00616784697222

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-