Catalog Number

84-14-4130

Brand Name

ZEOS

Version/Model Number

84-14-4130

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

HRX

Product Code Name

Arthroscope

Public Device Record Key

b6f38857-ec67-420a-9c38-2d6b53d8329a

Public Version Date

November 15, 2018

Public Version Number

2

DI Record Publish Date

August 24, 2018

Package DI Number

00812231030752

Quantity per Package

1

Contains DI Package

00812231030431

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Repair-Replace