Bio-Rad Laboratories, Inc. - Rubella IgM EIA - Bio-RAD Laboratories, Inc.

Duns Number:844766394

Device Description: Rubella IgM EIA

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More Product Details

Catalog Number

25174

Brand Name

Bio-Rad Laboratories, Inc.

Version/Model Number

25174

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

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K982281

Product Code Details

Product Code

LFX

Product Code Name

ENZYME LINKED IMMUNOABSORBENT ASSAY, RUBELLA

Device Record Status

Public Device Record Key

10d8dfd0-7186-49df-ae5e-4d7e6c40c137

Public Version Date

July 29, 2021

Public Version Number

5

DI Record Publish Date

September 12, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BIO-RAD LABORATORIES, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 98
3 A medical device with high risk that requires premarket approval 30