Catalog Number

-

Brand Name

ABX PENTRA DF 120

Version/Model Number

1280100006, 1280100007, 1280100008, 1280100010

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K050719

Product Code

GKZ

Product Code Name

Counter, Differential Cell

Public Device Record Key

7cfbdfcf-64d2-4309-bfdc-b7a2be3c4537

Public Version Date

September 16, 2022

Public Version Number

5

DI Record Publish Date

September 20, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-