Catalog Number

-

Brand Name

Mediplus

Version/Model Number

2309

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K031617,K031617

Product Code

KLA

Product Code Name

MONITOR, ESOPHAGEAL MOTILITY, AND TUBE

Public Device Record Key

45ec177e-1e58-41f2-b3e3-a49d148aa0c6

Public Version Date

August 05, 2022

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

15055140702811

Quantity per Package

10

Contains DI Package

05055140702814

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-