Catalog Number

-

Brand Name

DR -HOS

Version/Model Number

NN-CA-Blue

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

MNE

Product Code Name

Orthosis, Moldable, Supportive, Skin Protective

Public Device Record Key

028df4d5-9a91-486d-8686-eecdf3b8e90e

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

September 01, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-