Catalog Number

51614S

Brand Name

Magic3™ Hydrophilic Intermittent Catheter, Female

Version/Model Number

51614S

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

Yes

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

OHR

Product Code Name

Catheter care tray

Public Device Record Key

97b9e454-2e49-42e6-ba34-f4014ab90964

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 26, 2016

Package DI Number

10801741072496

Quantity per Package

50

Contains DI Package

00801741072499

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA