Catalog Number

-

Brand Name

CSH CANNULA

Version/Model Number

CSH-30019

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GEA

Product Code Name

CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

Public Device Record Key

7892ea5d-b27b-423e-9d32-d7cea291ae44

Public Version Date

April 16, 2018

Public Version Number

1

DI Record Publish Date

March 14, 2018

Package DI Number

14571225316618

Quantity per Package

120

Contains DI Package

04571225316611

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-