directCHECK Whole Blood Controls - directCHECK APTT - Abnormal 15/box - ACCRIVA DIAGNOSTICS HOLDINGS, INC.

Duns Number:079299318

Device Description: directCHECK APTT - Abnormal 15/box

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More Product Details

Catalog Number

DCJAPTT-A

Brand Name

directCHECK Whole Blood Controls

Version/Model Number

DCJAPTT-A

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K944691,K944691

Product Code Details

Product Code

GGN

Product Code Name

Plasma, Coagulation Control

Device Record Status

Public Device Record Key

226e50dd-6d6f-4ad6-9925-ff45df47e394

Public Version Date

August 31, 2022

Public Version Number

4

DI Record Publish Date

September 22, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ACCRIVA DIAGNOSTICS HOLDINGS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 6
2 A medical device with a moderate to high risk that requires special controls. 43