Catalog Number

1139101

Brand Name

Lifeshield

Version/Model Number

1139101

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FPK

Product Code Name

Tubing, fluid delivery

Public Device Record Key

1975fcfa-540a-4caf-9ed9-203acd7bba3e

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 01, 2016

Package DI Number

20887787005114

Quantity per Package

2

Contains DI Package

10887787005117

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case