Catalog Number

9890-000-30101

Brand Name

Philips MRC 880 CPO

Version/Model Number

9890-000-30101

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

ITY

Product Code Name

Assembly, tube housing, x-ray, diagnostic

Public Device Record Key

c682f024-b06a-4578-ad06-9d9a7b6b2faf

Public Version Date

December 10, 2020

Public Version Number

1

DI Record Publish Date

December 02, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-