Catalog Number

-

Brand Name

Enteral Feeding

Version/Model Number

TL-003

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

K895367,K895367

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

36faf90b-cb4b-4c6d-a304-319c3f9b3c89

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 22, 2016

Package DI Number

20020451101105

Quantity per Package

50

Contains DI Package

00020451101101

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-