Catalog Number

-

Brand Name

Tubing, Infusion Pump for Mediwatch Systems

Version/Model Number

TUBPTMDW

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)

Yes

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FEN

Product Code Name

DEVICE, CYSTOMETRIC, HYDRAULIC

Public Device Record Key

11108ffc-419a-403b-a6b8-039e4bc68aa8

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 01, 2017

Package DI Number

30627825010338

Quantity per Package

1000

Contains DI Package

20627825010331

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-