Catalog Number

ENT913

Brand Name

Medline

Version/Model Number

ENT913

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

-

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

KNT

Product Code Name

Tubes, gastrointestinal (and accessories)

Public Device Record Key

ca0ea429-d2c8-4e29-8ed7-46a86c1d050b

Public Version Date

January 18, 2021

Public Version Number

1

DI Record Publish Date

January 09, 2021

Package DI Number

20888277699813

Quantity per Package

10

Contains DI Package

10888277699816

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX