Catalog Number

-

Brand Name

Trinity Biotech

Version/Model Number

616434

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K935413

Product Code

LLL

Product Code Name

Extractable Antinuclear Antibody, Antigen And Control

Public Device Record Key

4ec7e882-4f8e-4212-860f-4255be0828bb

Public Version Date

January 03, 2020

Public Version Number

1

DI Record Publish Date

December 26, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-