AccuDiag™ - AccuDiag™ RF Latex Test KitFor the qualitative - Diagnostic Automation, Inc.

Duns Number:878252071

Device Description: AccuDiag™ RF Latex Test KitFor the qualitative and semi-quantitative measurement of RF in AccuDiag™ RF Latex Test KitFor the qualitative and semi-quantitative measurement of RF in human serum.

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More Product Details

Catalog Number

320-100

Brand Name

AccuDiag™

Version/Model Number

DACD320-100

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

-

Product Code Details

Product Code

DHR

Product Code Name

System, Test, Rheumatoid Factor

Device Record Status

Public Device Record Key

1470b6ce-2049-4ea7-896b-6da9ec829078

Public Version Date

September 03, 2021

Public Version Number

1

DI Record Publish Date

August 26, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"DIAGNOSTIC AUTOMATION, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 7
2 A medical device with a moderate to high risk that requires special controls. 16