Catalog Number

MPL2-1030H

Brand Name

GP General Purpose Drainage Catheter

Version/Model Number

MPL2-1030H

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

February 28, 2027

Issuing Agency

In HIBCC

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

GBO

Product Code Name

Catheter, Nephrostomy, General & Plastic Surgery

Public Device Record Key

1c8e009e-64e1-47bd-b27d-8e595f8b49a1

Public Version Date

April 29, 2022

Public Version Number

4

DI Record Publish Date

August 29, 2016

Package DI Number

H862MPL21030H2

Quantity per Package

6

Contains DI Package

H862MPL21030H1

Package Discontinue Date

February 28, 2027

Package Status

In Commercial Distribution

Package Type

Shipper