Catalog Number

412036

Brand Name

Laguna Nigel 110V

Version/Model Number

412036

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

LGX

Product Code Name

Table, Examination, Medical, Powered

Public Device Record Key

4f84221e-f9ef-467d-b9a4-06fa657e299d

Public Version Date

August 14, 2018

Public Version Number

3

DI Record Publish Date

July 18, 2017

Package DI Number

00667259000511

Quantity per Package

1

Contains DI Package

00667259000108

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

skid