Catalog Number

1252.232G

Brand Name

Nutriline Twinflo

Version/Model Number

1252.232G

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

K052475,K052475,K052475

Product Code

LJS

Product Code Name

Catheter, intravascular, therapeutic, long-term greater than 30 days

Public Device Record Key

009bf2fb-c2a4-43a3-894d-f9516561a212

Public Version Date

February 19, 2021

Public Version Number

2

DI Record Publish Date

March 13, 2020

Package DI Number

30849884000840

Quantity per Package

10

Contains DI Package

00849884000849

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-