Catalog Number

-

Brand Name

TriplePlay

Version/Model Number

10-21001-0301

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K990321,K990321,K990321

Product Code

MNR

Product Code Name

Ventilatory Effort Recorder

Public Device Record Key

76fb614f-94cf-47c5-a125-c24427413d0a

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

October 13, 2016

Package DI Number

20817377020104

Quantity per Package

50

Contains DI Package

00817377020100

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-