Catalog Number

-

Brand Name

PerAldecide

Version/Model Number

Gallons

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 29, 2018

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

LRJ

Product Code Name

Disinfectant, Medical Devices

Public Device Record Key

225cb398-e0b2-4b11-a5fe-0391395c614e

Public Version Date

March 19, 2021

Public Version Number

6

DI Record Publish Date

September 24, 2016

Package DI Number

00857635006033

Quantity per Package

4

Contains DI Package

00857635006026

Package Discontinue Date

September 29, 2018

Package Status

Not in Commercial Distribution

Package Type

-