Blu Blade - ISORAY MEDICAL, INC.

Duns Number:113577485

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More Product Details

Catalog Number

-

Brand Name

Blu Blade

Version/Model Number

BB-1

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

IWJ

Product Code Name

System, Applicator, Radionuclide, Manual

Device Record Status

Public Device Record Key

6be38e79-333b-4805-b061-ce0710e9d1d8

Public Version Date

April 05, 2019

Public Version Number

1

DI Record Publish Date

March 28, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ISORAY MEDICAL, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 4
2 A medical device with a moderate to high risk that requires special controls. 17