Catalog Number

0702-020-000

Brand Name

Neptune 2

Version/Model Number

0702020000

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

-

Product Code

JCX

Product Code Name

APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED

Public Device Record Key

e522d440-14c1-445e-8946-ce06fe47a58c

Public Version Date

May 05, 2022

Public Version Number

5

DI Record Publish Date

September 23, 2016

Package DI Number

37613154688280

Quantity per Package

20

Contains DI Package

07613154688289

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pack