Catalog Number

5162

Brand Name

N/A

Version/Model Number

N/A

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

HMX

Product Code Name

Cannula, Ophthalmic

Public Device Record Key

03780dbb-9203-4dc6-8351-278528be20d4

Public Version Date

October 07, 2019

Public Version Number

6

DI Record Publish Date

April 04, 2018

Package DI Number

30818255010641

Quantity per Package

5

Contains DI Package

10818255010647

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton