Catalog Number

-

Brand Name

Portex

Version/Model Number

C48201813D-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)

Yes

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

b63eaba6-7b9f-45ab-80f2-52c8719fd22e

Public Version Date

October 24, 2022

Public Version Number

3

DI Record Publish Date

June 07, 2018

Package DI Number

35019517145360

Quantity per Package

20

Contains DI Package

15019517145366

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX