Catalog Number

214120

Brand Name

NA

Version/Model Number

214120

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

GEA

Product Code Name

CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

Public Device Record Key

4f16c9cb-da6f-4fb6-9031-36b9cca51f00

Public Version Date

July 22, 2020

Public Version Number

3

DI Record Publish Date

September 01, 2015

Package DI Number

20886705003614

Quantity per Package

5

Contains DI Package

10886705003617

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

PACKAGE