ABX PENTRA 60C+ - HORIBA ABX SAS

Duns Number:273647420

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More Product Details

Catalog Number

-

Brand Name

ABX PENTRA 60C+

Version/Model Number

1280120006, 1280120008

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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

K030144

Product Code Details

Product Code

GKZ

Product Code Name

Counter, Differential Cell

Device Record Status

Public Device Record Key

c9fc9cce-ea25-4500-94b2-2e7d15235b3f

Public Version Date

September 16, 2022

Public Version Number

5

DI Record Publish Date

September 02, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HORIBA ABX SAS" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 104
2 A medical device with a moderate to high risk that requires special controls. 100