Catalog Number

-

Brand Name

Uterine ElevatOR PRO with Long Handle

Version/Model Number

UE-LHPRO-32

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

LKF

Product Code Name

Cannula, Manipulator/Injector, Uterine

Public Device Record Key

2f092829-7a94-4f60-a2e5-4272d1bbcbc7

Public Version Date

October 03, 2019

Public Version Number

1

DI Record Publish Date

September 25, 2019

Package DI Number

09349967000922

Quantity per Package

6

Contains DI Package

09349967000915

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipper Box