Catalog Number

-

Brand Name

25GA Flexible 41GA Cannula

Version/Model Number

PD225.41

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"

Yes

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

2ea4b075-5929-471c-9fef-1ca691bb07a3

Public Version Date

October 07, 2019

Public Version Number

6

DI Record Publish Date

May 06, 2016

Package DI Number

10632307001533

Quantity per Package

5

Contains DI Package

00632307001536

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box