Catalog Number

C-008.33.601

Brand Name

OMEGA 600 wired

Version/Model Number

000

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

HLI

Product Code Name

Ophthalmoscope, Ac-Powered

Public Device Record Key

981a4cb3-d095-419b-94c8-9b5c029e65c6

Public Version Date

February 19, 2021

Public Version Number

3

DI Record Publish Date

January 13, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-