Catalog Number

S218

Brand Name

Single Use Surgical Professional

Version/Model Number

S218

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

KDD

Product Code Name

Kit, Surgical Instrument, Disposable

Public Device Record Key

b97a3a85-0969-455a-85d0-8df6a5e67509

Public Version Date

June 17, 2022

Public Version Number

5

DI Record Publish Date

August 09, 2016

Package DI Number

05055299103258

Quantity per Package

25

Contains DI Package

05055299103227

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton