Catalog Number

-

Brand Name

Disposable Direct Image Flat (VFD)

Version/Model Number

VFD

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

HJK

Product Code Name

Lens, Contact, Polymethylmethacrylate, Diagnostic

Public Device Record Key

132e66c2-c100-4e0f-a8c9-d5ce9cc2190c

Public Version Date

September 30, 2020

Public Version Number

4

DI Record Publish Date

September 29, 2016

Package DI Number

10811608017225

Quantity per Package

10

Contains DI Package

00811608017228

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX