Catalog Number

PRI.31G2

Brand Name

PRIMODENT

Version/Model Number

PRI.31G2

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

MRI safety Status

MR Safe

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

ELM

Product Code Name

Denture, plastic, teeth

Public Device Record Key

cc98c1af-bede-45ad-9b12-b20746eb8e7a

Public Version Date

June 22, 2021

Public Version Number

1

DI Record Publish Date

June 14, 2021

Package DI Number

EPOLPRI31G203

Quantity per Package

1

Contains DI Package

EPOLPRI31G2

Package Discontinue Date

June 14, 2021

Package Status

Not in Commercial Distribution

Package Type

plastic card