ImmunoCAP Autoimmunity Specific IgG Sample Diluent - ImmunoCAP Autoimmunity Specific IgG Sample Diluent - Phadia AB

Duns Number:354019424

Device Description: ImmunoCAP Autoimmunity Specific IgG Sample Diluent

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More Product Details

Catalog Number

34-2316-11

Brand Name

ImmunoCAP Autoimmunity Specific IgG Sample Diluent

Version/Model Number

34-2316-11

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

K072661,K072661

Product Code Details

Product Code

JJY

Product Code Name

Multi-analyte controls, all kinds (assayed)

Device Record Status

Public Device Record Key

6cb0e2b4-4aea-49fb-a4a2-b0fae820e6a7

Public Version Date

April 05, 2019

Public Version Number

1

DI Record Publish Date

March 28, 2019

Additional Identifiers

Package DI Number

07333066000749

Quantity per Package

6

Contains DI Package

07333066019840

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"PHADIA AB" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 225
2 A medical device with a moderate to high risk that requires special controls. 518