Catalog Number

-

Brand Name

ExactEtch

Version/Model Number

2120K

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

HNN

Product Code Name

Knife, Ophthalmic

Public Device Record Key

587dc62f-ccce-4a24-bb65-410600c05238

Public Version Date

November 01, 2019

Public Version Number

1

DI Record Publish Date

October 24, 2019

Package DI Number

00813059010032

Quantity per Package

6

Contains DI Package

00813059010711

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box