Catalog Number

-

Brand Name

Bi Manual Curved set 0.4mm side ports

Version/Model Number

92-3000

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

38d506be-1bd0-4251-8c82-9c61afb9369f

Public Version Date

October 07, 2019

Public Version Number

6

DI Record Publish Date

June 29, 2017

Package DI Number

10848782024350

Quantity per Package

10

Contains DI Package

00848782024353

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box