Volumat™ Line - Fresenius Kabi AG

Duns Number:315654579

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More Product Details

Catalog Number

M46443450

Brand Name

Volumat™ Line

Version/Model Number

VL SP 62-1

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

40769d6e-ef5c-42ca-a2a1-830a0d596722

Public Version Date

September 07, 2022

Public Version Number

4

DI Record Publish Date

September 24, 2016

Additional Identifiers

Package DI Number

4250273714821

Quantity per Package

30

Contains DI Package

04250273714838

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