Catalog Number

-

Brand Name

Wolf X-Ray

Version/Model Number

10011

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

EAM

Product Code Name

Screen, Intensifying, Radiographic

Public Device Record Key

a00749c0-4f0e-4ac5-9ee2-3c966ad28410

Public Version Date

October 05, 2020

Public Version Number

1

DI Record Publish Date

September 26, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-