Optilite Albumin Kit - THE BINDING SITE GROUP LIMITED

Duns Number:347045614

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More Product Details

Catalog Number

-

Brand Name

Optilite Albumin Kit

Version/Model Number

NK032.OPT.A

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

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

DCF

Product Code Name

Albumin, Antigen, Antiserum, Control

Device Record Status

Public Device Record Key

7d1664d2-5443-48bc-b640-2dc985efc7e2

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

September 24, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"THE BINDING SITE GROUP LIMITED" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 85
2 A medical device with a moderate to high risk that requires special controls. 183