Catalog Number

18069

Brand Name

Synergetics

Version/Model Number

18069

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

KDD

Product Code Name

Kit, Surgical Instrument, Disposable

Public Device Record Key

e127602a-048b-480c-928f-2246449ea3cd

Public Version Date

June 08, 2020

Public Version Number

1

DI Record Publish Date

May 31, 2020

Package DI Number

20841305107605

Quantity per Package

10

Contains DI Package

10841305101125

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box