QuikScreen - SYNTRON BIORESEARCH, INC.

Duns Number:174517060

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More Product Details

Catalog Number

-

Brand Name

QuikScreen

Version/Model Number

60A41

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

K130275,K130275,K071489,K071489,K130275,K071489

Product Code Details

Product Code

DIO

Product Code Name

Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Device Record Status

Public Device Record Key

5f8013aa-d65c-4780-a6b7-eb3f0db68a2b

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

May 15, 2017

Additional Identifiers

Package DI Number

20748349000346

Quantity per Package

4

Contains DI Package

10748349000349

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"SYNTRON BIORESEARCH, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2
2 A medical device with a moderate to high risk that requires special controls. 28