Catalog Number

9903R

Brand Name

Medline

Version/Model Number

9903R

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

HST

Product Code Name

Apparatus, traction, non-powered

Public Device Record Key

afced1bd-ee31-4b5e-ac27-ff36c5aeb939

Public Version Date

May 23, 2022

Public Version Number

1

DI Record Publish Date

May 13, 2022

Package DI Number

20888277383309

Quantity per Package

10

Contains DI Package

10888277383302

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE