Catalog Number

LBF-502-340

Brand Name

DANmed

Version/Model Number

LBF-502-340

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 31, 2022

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

-

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

HET

Product Code Name

LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)

Public Device Record Key

0c0acf50-4251-4bb0-81a5-9c1ab4b32eb8

Public Version Date

August 31, 2022

Public Version Number

3

DI Record Publish Date

March 15, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-