Catalog Number

TDC-5.0

Brand Name

Tools

Version/Model Number

TDC-5.0

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NDP

Product Code Name

Accessories, Implant, Dental, Endosseous

Public Device Record Key

2f0ace0a-805a-4150-b845-d39332904806

Public Version Date

January 09, 2020

Public Version Number

2

DI Record Publish Date

October 07, 2019

Package DI Number

17290111274586

Quantity per Package

10

Contains DI Package

07290111274589

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

bag