Catalog Number

ML8001VS

Brand Name

Vacuum Tubing

Version/Model Number

ML8001VS

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

KYG

Product Code Name

Device, Irrigation, Ocular Surgery

Public Device Record Key

a1025d8b-a9bf-462f-8713-cf570c116317

Public Version Date

July 04, 2022

Public Version Number

2

DI Record Publish Date

August 28, 2020

Package DI Number

10850724001107

Quantity per Package

10

Contains DI Package

00850724001100

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Bag