COULTER Ac•T 5diff Fix - COULTER Ac•T 5diff Fix - Beckman Coulter, Inc.

Duns Number:008254708

Device Description: COULTER Ac•T 5diff Fix

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More Product Details

Catalog Number

8547171

Brand Name

COULTER Ac•T 5diff Fix

Version/Model Number

8547171

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

GGK

Product Code Name

Products, Red-Cell Lysing Products

Device Record Status

Public Device Record Key

9314c664-f16c-4c13-8d4c-abb4af6a95d4

Public Version Date

September 08, 2020

Public Version Number

1

DI Record Publish Date

August 31, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BECKMAN COULTER, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 319
2 A medical device with a moderate to high risk that requires special controls. 503
3 A medical device with high risk that requires premarket approval 9
U Unclassified 1