CT Exprès™ - Day Set III HP - Bracco Injeneering SA

Duns Number:482489007

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More Product Details

Catalog Number

640460

Brand Name

CT Exprès™ - Day Set III HP

Version/Model Number

640460

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K151048,K151048

Product Code Details

Product Code

IZQ

Product Code Name

Injector, Contrast Medium, Automatic

Device Record Status

Public Device Record Key

5ecd7f5f-7786-4722-ad5b-5e8e62b5cee2

Public Version Date

April 20, 2020

Public Version Number

4

DI Record Publish Date

September 20, 2016

Additional Identifiers

Package DI Number

37630039300020

Quantity per Package

15

Contains DI Package

17630039300026

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"BRACCO INJENEERING SA" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 84