ABACUS - ABACUS 3.3 CE - BAXTER HEALTHCARE CORPORATION

Duns Number:005083209

Device Description: ABACUS 3.3 CE

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More Product Details

Catalog Number

83003391

Brand Name

ABACUS

Version/Model Number

83003391

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

May 31, 2029

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

NEP

Product Code Name

SYSTEM/DEVICE, PHARMACY COMPOUNDING

Device Record Status

Public Device Record Key

65c8e2b2-86b4-4733-8698-435ff1da61ae

Public Version Date

October 11, 2022

Public Version Number

4

DI Record Publish Date

July 01, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BAXTER HEALTHCARE CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 16
2 A medical device with a moderate to high risk that requires special controls. 101
3 A medical device with high risk that requires premarket approval 19