Catalog Number

-

Brand Name

Portex

Version/Model Number

C49201781D-NL

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"

Yes

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

BTC

Product Code Name

BAG, RESERVOIR

Public Device Record Key

779860d2-d6a7-4ecf-aee9-1e7060cc4d34

Public Version Date

October 24, 2022

Public Version Number

4

DI Record Publish Date

November 07, 2016

Package DI Number

35019517059872

Quantity per Package

20

Contains DI Package

15019517059878

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX