RDS - RDS bulk pack - AMERICAN BIO MEDICA CORPORATION

Duns Number:966665036

Device Description: RDS bulk pack THC/COC/OPI300/METH/MDMA/PCP/OXY/AMP/BZO/MTD

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More Product Details

Catalog Number

10-10SPB-177

Brand Name

RDS

Version/Model Number

10-10SPB-177

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

K002447,K002447

Product Code Details

Product Code

DIO

Product Code Name

Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Device Record Status

Public Device Record Key

0230ea14-e30e-47c6-87f3-9b22252002f6

Public Version Date

July 06, 2018

Public Version Number

2

DI Record Publish Date

May 23, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"AMERICAN BIO MEDICA CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1
2 A medical device with a moderate to high risk that requires special controls. 6