Catalog Number

-

Brand Name

25GA Soft Tip Cannula

Version/Model Number

PD225.00

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

1da778ca-082b-4e37-89b5-877c19690d65

Public Version Date

October 07, 2019

Public Version Number

6

DI Record Publish Date

May 06, 2016

Package DI Number

10632307001519

Quantity per Package

10

Contains DI Package

00632307001512

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box