Catalog Number

SMA3ILDIPH

Brand Name

CARDINAL HEALTH

Version/Model Number

SMA3ILDIPH

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

HCY

Product Code Name

CURETTE, UTERINE

Public Device Record Key

b4984edd-626f-44ef-b0f6-0a084bfc5e9f

Public Version Date

March 07, 2019

Public Version Number

1

DI Record Publish Date

February 04, 2019

Package DI Number

50888439280393

Quantity per Package

2

Contains DI Package

10888439280395

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE