Catalog Number

-

Brand Name

QUINTAPOINT

Version/Model Number

10167252

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)

Yes

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

61d59f74-7652-4bdb-8a17-91e4fcdd34d7

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

January 16, 2017

Package DI Number

20087701428894

Quantity per Package

24

Contains DI Package

10087701428897

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case