Catalog Number

191-950

Brand Name

Epimed

Version/Model Number

191-950

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

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

LRO

Product Code Name

General surgery tray

Public Device Record Key

9b1d28c2-e318-4043-9d95-e1f563160e13

Public Version Date

September 16, 2022

Public Version Number

8

DI Record Publish Date

October 24, 2017

Package DI Number

10818788021523

Quantity per Package

10

Contains DI Package

00818788021526

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case