Catalog Number

08N47-095

Brand Name

Alinity m

Version/Model Number

08N47-095

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

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

MKT

Product Code Name

Hepatitis Viral B DNA Detection

Public Device Record Key

b780c885-b801-45dc-a062-8f3a459ed5dd

Public Version Date

April 21, 2021

Public Version Number

2

DI Record Publish Date

September 23, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-