Catalog Number

ENF30-KMS

Brand Name

Ameritus ENFit

Version/Model Number

ENF30-KMS

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

K110853,K162188,K110853,K162188,K110853,K162188

Product Code

PNR

Product Code Name

Enteral Syringes With Enteral Specific Connectors

Public Device Record Key

3090e5e8-5ee4-44b9-8830-64de3fbc1582

Public Version Date

October 29, 2021

Public Version Number

7

DI Record Publish Date

August 03, 2016

Package DI Number

30817522012777

Quantity per Package

400

Contains DI Package

10817522012773

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case