Catalog Number

50745-002

Brand Name

Infinity

Version/Model Number

1

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 03, 2021

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LZH

Product Code Name

Pump, Infusion, Enteral

Public Device Record Key

53733408-185e-4c82-a1a6-cae8e1929d90

Public Version Date

May 07, 2021

Public Version Number

5

DI Record Publish Date

August 03, 2018

Package DI Number

38148440000112

Quantity per Package

3

Contains DI Package

18148440000118

Package Discontinue Date

March 03, 2021

Package Status

Not in Commercial Distribution

Package Type

-