Catalog Number

CPRMP30

Brand Name

Medline Industries, Inc.

Version/Model Number

CPRMP30

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)

-

Device labeled as "Not made with natural rubber latex"

Yes

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

BYE

Product Code Name

Attachment, breathing, positive end expiratory pressure

Public Device Record Key

f8ee68ed-36cd-4aeb-813c-af3314385926

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 15, 2015

Package DI Number

40884389126043

Quantity per Package

20

Contains DI Package

10884389126042

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-