Catalog Number

-

Brand Name

Hu Capsular Polisher

Version/Model Number

12-2685

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

-

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

HND

Product Code Name

Spatula, ophthalmic

Public Device Record Key

2d593636-52e9-4ca5-bf70-b8f2edbaf50f

Public Version Date

February 11, 2022

Public Version Number

1

DI Record Publish Date

February 03, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-