Catalog Number

800-0091

Brand Name

SchureMed

Version/Model Number

800-0091

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

-

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

FWZ

Product Code Name

Operating Room Accessories Table Tray

Public Device Record Key

a2d541b9-3f3f-4465-80a4-f7e291e3edb2

Public Version Date

June 03, 2021

Public Version Number

2

DI Record Publish Date

February 25, 2019

Package DI Number

01810014600085

Quantity per Package

1

Contains DI Package

00810014600086

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-