Volumat™ Line M46445780

GUDID 04250273731972

Fresenius Kabi AG

Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use Electric infusion pump administration set, single-use
Primary Device ID04250273731972
NIH Device Record Key4b5e0a7f-5308-4c43-a5e4-ec4745eba112
Commercial Distribution StatusIn Commercial Distribution
Brand NameVolumat™ Line
Version Model NumberVL PR44-12
Catalog NumberM46445780
Company DUNS315654579
Company NameFresenius Kabi AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+496621168400
Emailheinrich.martens@fresenius-kab
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com
Phone+496621168400
Emailheinrich.martens@fresenius-kabi.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104250273731965 [Primary]
GS104250273731972 [Package]
Contains: 04250273731965
Package: Box [30 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FRNPump, Infusion
MRZAccessories, Pump, Infusion

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-06-25
Device Publish Date2018-05-24

On-Brand Devices [Volumat™ Line]

04250273733891For use with the Volumat primary lines.
04250273733860For use with Agilia VP MC pumps / Volumat MC Agilia pump or gravity only.
04250273731972VL PR44-12
04250273731958VL PR40-11
04250273731910VL ST10-X0
04250273731897VL SL00-X0
04250273731873VL ON72-X1
04250273731859VL ST02-X0
4250273714821VL SP 62-1
04250273714517VL ST 10-0
4250273714500VL PA 92-1
4250273714487VL SL 00-0
4250273714463VL TR 00-0
4250273714449VL PR 42-41
4250273714401VL ON 72-1
4250273714388VL PN 02-1
4250273714364VL PR 42-12
4250273714340VL PR 72-11
4250273714326VL PA 92-2
4250273714302VL PR 42-21
4250273714289VL ST 02-0
4250273714265VL PR 42-11
04250273714234VL PR 22-1
4250273714197VL SP 22-0

Trademark Results [Volumat]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VOLUMAT
VOLUMAT
79053901 3587415 Dead/Cancelled
Fresenius Kabi AG
2008-04-03

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