Catalog Number

72F1013-1-24

Brand Name

Medline/MMS Sales

Version/Model Number

72F1013-1-24

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

Yes

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

-

Product Code

CAI

Product Code Name

Circuit, breathing (w connector, adaptor, y piece)

Public Device Record Key

26737c96-f35e-40a4-8dbe-09b08b91bb07

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

November 07, 2016

Package DI Number

20888277638324

Quantity per Package

20

Contains DI Package

10888277638327

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

cs