Catalog Number

-

Brand Name

Vera PDI

Version/Model Number

PDIH

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

K915249

Product Code

EJH

Product Code Name

Alloy, Metal, Base

Public Device Record Key

43bc2c06-2dc0-49da-8f99-49b9ce8f7c2e

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

January 08, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-