Catalog Number

6571749

Brand Name

QC-WBS-GED

Version/Model Number

QC-WBS-GED

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 02, 2021

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

IXQ

Product Code Name

Table, radiographic, stationary top

Public Device Record Key

240d8816-2f8e-4242-9f8a-18826dd45491

Public Version Date

November 04, 2021

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-