Catalog Number

-

Brand Name

EasyTouch

Version/Model Number

831050

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FMF

Product Code Name

Syringe, Piston

Public Device Record Key

e5aa6af3-3944-4b1d-ab44-a70f94546e2a

Public Version Date

September 12, 2018

Public Version Number

3

DI Record Publish Date

August 05, 2016

Package DI Number

MHC8310502

Quantity per Package

50

Contains DI Package

MHC18310501

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-