Catalog Number

-

Brand Name

Vertex-Dental BV

Version/Model Number

NOWHHCMN301000

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

DYT

Product Code Name

MAINTAINER, SPACE PREFORMED, ORTHODONTIC

Public Device Record Key

0cdeba22-e889-4742-8049-3f798515cd5e

Public Version Date

October 29, 2021

Public Version Number

5

DI Record Publish Date

March 15, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-