Catalog Number

70-0062-218

Brand Name

Gastrostomy Tube - Dual ENFit Port (Tri-Funnel)

Version/Model Number

VED-218

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

K142075,K142075

Product Code

PIF

Product Code Name

Gastrointestinal Tubes With Enteral Specific Connectors

Public Device Record Key

78acaca6-76fa-4d19-b3cb-96e5ae0ce998

Public Version Date

April 20, 2020

Public Version Number

5

DI Record Publish Date

August 08, 2016

Package DI Number

10813939024934

Quantity per Package

5

Contains DI Package

00813939024937

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case Box