Catalog Number

-

Brand Name

EasyTouch

Version/Model Number

830555

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

ebe0a8fb-0418-433b-a117-43d5cb94d78a

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 10, 2016

Package DI Number

MHC18305552

Quantity per Package

10

Contains DI Package

MHC18305551

Package Discontinue Date

-

Package Status

-

Package Type

-