Catalog Number

ZMMF

Brand Name

PadPro

Version/Model Number

ZMMF

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

P200004

Product Code

MKJ

Product Code Name

Automated external defibrillators (non-wearable)

Public Device Record Key

132a7340-5427-4bd3-8e51-b82bfeab6002

Public Version Date

November 16, 2021

Public Version Number

1

DI Record Publish Date

November 08, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-