TheraSphere Administration Accessory Kit - For use with a TheraSphere Administration Set to - BIOCOMPATIBLES UK LTD

Duns Number:222870839

Device Description: For use with a TheraSphere Administration Set to administer TheraSphere Y90 Glass Microsph For use with a TheraSphere Administration Set to administer TheraSphere Y90 Glass Microspheres

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More Product Details

Catalog Number

-

Brand Name

TheraSphere Administration Accessory Kit

Version/Model Number

k125914-001

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 22, 2020

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

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

NAW

Product Code Name

Microspheres Radionuclide

Device Record Status

Public Device Record Key

30a8ee87-cf0c-427e-960b-3a0a7719d24b

Public Version Date

September 29, 2021

Public Version Number

4

DI Record Publish Date

September 24, 2014

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BIOCOMPATIBLES UK LTD" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 9
3 A medical device with high risk that requires premarket approval 73