Catalog Number

395

Brand Name

ADC®

Version/Model Number

395

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FTY

Product Code Name

Tape, Measuring, Rulers And Calipers

Public Device Record Key

e282969d-6ddd-4e0c-910a-d9c87334f17c

Public Version Date

June 11, 2018

Public Version Number

3

DI Record Publish Date

September 21, 2016

Package DI Number

00634782501907

Quantity per Package

20

Contains DI Package

00634782801908

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case