Catalog Number

-

Brand Name

Ezy Dose

Version/Model Number

67015/HK67015

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

OHY

Product Code Name

Pill Crusher/Cutter

Public Device Record Key

d3a1e686-d478-464c-b9e1-e843773fd112

Public Version Date

November 30, 2020

Public Version Number

1

DI Record Publish Date

November 20, 2020

Package DI Number

20025715670151

Quantity per Package

6

Contains DI Package

00025715670157

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

INNER