Catalog Number

-

Brand Name

PiSA BioPharm

Version/Model Number

600205

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

KPE

Product Code Name

Container, I.V.

Public Device Record Key

8fb16532-21f4-4e56-88d6-35d1980f6071

Public Version Date

October 23, 2019

Public Version Number

2

DI Record Publish Date

September 24, 2018

Package DI Number

00850002046120

Quantity per Package

50

Contains DI Package

00850002046045

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case