Catalog Number

-

Brand Name

Poly Rb A-Hu C4c Complement/FITC

Version/Model Number

F0169

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

DBI

Product Code Name

COMPLEMENT C4, ANTIGEN, ANTISERUM, CONTROL

Public Device Record Key

44bb011e-fa35-454c-8cb8-6183e201d45a

Public Version Date

December 07, 2020

Public Version Number

8

DI Record Publish Date

September 16, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-