Catalog Number

-

Brand Name

LCCS

Version/Model Number

ET22125-LC

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

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

K131006,K131006,K131006

Product Code

BSP

Product Code Name

Needle, Conduction, Anesthetic (W/Wo Introducer)

Public Device Record Key

ecabb1f8-23d4-48bd-a98f-1cf4c595f325

Public Version Date

August 02, 2021

Public Version Number

1

DI Record Publish Date

July 24, 2021

Package DI Number

14895233608023

Quantity per Package

25

Contains DI Package

04895233608026

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box