Catalog Number

-

Brand Name

MD Flex heaby body

Version/Model Number

9284

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 31, 2019

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K134008

Product Code

ELW

Product Code Name

Material, Impression

Public Device Record Key

b619ab9a-6706-497c-815d-e26fd7f84482

Public Version Date

January 24, 2022

Public Version Number

4

DI Record Publish Date

May 01, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-