Catalog Number

-

Brand Name

N/A

Version/Model Number

ACTIONII ARM

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

-

Product Code

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

0a04f4f5-8dfc-42fd-b44f-94015dcc5b8e

Public Version Date

July 26, 2021

Public Version Number

4

DI Record Publish Date

July 27, 2017

Package DI Number

08809447651866

Quantity per Package

1

Contains DI Package

08809447651859

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton Box