Catalog Number

682002/B

Brand Name

Meritrans DTXPlus®

Version/Model Number

10884450371739

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

DXN

Product Code Name

System, measurement, blood-pressure, non-invasive

Public Device Record Key

d68c48c7-fc30-48cd-81b3-6307ecf1601a

Public Version Date

December 13, 2021

Public Version Number

2

DI Record Publish Date

October 12, 2021

Package DI Number

20884450371736

Quantity per Package

10

Contains DI Package

10884450371739

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-