Catalog Number

U-20210K

Brand Name

One Step Plus U/D (60) KIT

Version/Model Number

U-20210K

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 01, 2017

Issuing Agency

In HIBCC

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

EMA

Product Code Name

CEMENT, DENTAL

Public Device Record Key

e89b1bc8-6ef5-46f4-a50a-0f61648c12b9

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 12, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-