Catalog Number

-

Brand Name

Medela

Version/Model Number

ENPU2050

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"

Yes

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

K102548,K102548,K102548

Product Code

KNT

Product Code Name

Tubes, Gastrointestinal (And Accessories)

Public Device Record Key

f7b07983-20db-425a-8199-b2cbd3598ab9

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 16, 2017

Package DI Number

10859950007297

Quantity per Package

10

Contains DI Package

00859950007290

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton