Volumat™ Line - Fresenius Kabi AG

Duns Number:315654579

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More Product Details

Catalog Number

M46445780

Brand Name

Volumat™ Line

Version/Model Number

VL PR44-12

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K121613,K121613

Product Code Details

Product Code

FRN

Product Code Name

Pump, Infusion

Device Record Status

Public Device Record Key

4b5e0a7f-5308-4c43-a5e4-ec4745eba112

Public Version Date

September 07, 2022

Public Version Number

3

DI Record Publish Date

May 24, 2018

Additional Identifiers

Package DI Number

04250273731972

Quantity per Package

30

Contains DI Package

04250273731965

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"FRESENIUS KABI AG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 5
2 A medical device with a moderate to high risk that requires special controls. 87
U Unclassified 2