Catalog Number

0215-030-000

Brand Name

NA

Version/Model Number

0215030000

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 01, 2019

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

GCY

Product Code Name

APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED

Public Device Record Key

8f828eed-551a-43db-9321-1caa1c30934c

Public Version Date

February 19, 2020

Public Version Number

2

DI Record Publish Date

September 24, 2018

Package DI Number

34546540185014

Quantity per Package

10

Contains DI Package

04546540185013

Package Discontinue Date

April 01, 2019

Package Status

Not in Commercial Distribution

Package Type

pack