Catalog Number

-

Brand Name

CAREFINE

Version/Model Number

1100013

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

bb1ce498-5907-4152-95e2-d0fb31a258db

Public Version Date

July 03, 2019

Public Version Number

3

DI Record Publish Date

March 10, 2017

Package DI Number

20894743001745

Quantity per Package

30

Contains DI Package

00894743001741

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case