Catalog Number

-

Brand Name

MALE/FEMALE LUERLOCK

Version/Model Number

LL03-01

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"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

JRJ

Product Code Name

Unit, Drying

Public Device Record Key

8c25bcce-5e64-4dda-8dbc-65172c70ad66

Public Version Date

October 02, 2020

Public Version Number

1

DI Record Publish Date

September 24, 2020

Package DI Number

10843356102540

Quantity per Package

100

Contains DI Package

00843356102543

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-