uTASWako AFP-L3 Sample Dilution Buffer - In-Vitro Diagnostic Use - FUJIFILM WAKO PURE CHEMICAL CORPORATION

Duns Number:690598875

Device Description: In-Vitro Diagnostic Use

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

997-61501

Brand Name

uTASWako AFP-L3 Sample Dilution Buffer

Version/Model Number

997-61501

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 23, 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

Yes

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

K100464,K100464

Product Code Details

Product Code

NSF

Product Code Name

Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment

Device Record Status

Public Device Record Key

65b851f1-6e77-4b88-afd2-dbc81837227c

Public Version Date

October 26, 2020

Public Version Number

5

DI Record Publish Date

December 22, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"FUJIFILM WAKO PURE CHEMICAL CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 18
2 A medical device with a moderate to high risk that requires special controls. 22