Catalog Number

AG 0400PDCI

Brand Name

HERCULES II

Version/Model Number

CPL

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

ING

Product Code Name

Elevator, wheelchair, portable

Public Device Record Key

4679af5f-da46-4cda-a50d-2d9bd10fb954

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

May 06, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-