Catalog Number

-

Brand Name

SUPEREAGLE

Version/Model Number

31302

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 31, 2017

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

LZU

Product Code Name

Plug, Punctum

Public Device Record Key

efce6e14-a4ca-4a9c-9d2c-493222a2b4a6

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 26, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-