Catalog Number

72200731R

Brand Name

Medline

Version/Model Number

72200731R

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

Yes

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

bda28218-0163-448e-a7a3-07e595b7427c

Public Version Date

July 04, 2022

Public Version Number

2

DI Record Publish Date

May 12, 2022

Package DI Number

20888277388502

Quantity per Package

6

Contains DI Package

10888277388505

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE