Catalog Number

001-282

Brand Name

PRO-TEC PIG

Version/Model Number

001-282

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

IWR

Product Code Name

Holder, Syringe, Lead

Public Device Record Key

0857f926-e88c-48ae-85ee-1ac6a2a72cf0

Public Version Date

April 22, 2019

Public Version Number

1

DI Record Publish Date

April 12, 2019

Package DI Number

10718175000837

Quantity per Package

6

Contains DI Package

00718175000830

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box