Catalog Number

S219

Brand Name

Single Use Surgical Professional

Version/Model Number

S219

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

GCX

Product Code Name

Apparatus, Suction, Operating-Room, Wall Vacuum Powered

Public Device Record Key

96cd82d4-3ea0-4916-a5f7-401e1a34b1bc

Public Version Date

April 20, 2020

Public Version Number

4

DI Record Publish Date

August 09, 2016

Package DI Number

05055299103272

Quantity per Package

10

Contains DI Package

05055299103241

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton