Dispenser DP 30

GUDID ENOU4180US0

Infiltration pump

Nouvag AG

Bedside infusion pump, single-channel
Primary Device IDENOU4180US0
NIH Device Record Key21333050-e060-44a5-a86b-7302e408b83c
Commercial Distribution StatusIn Commercial Distribution
Brand NameDispenser DP 30
Version Model Number4180US
Company DUNS480610476
Company NameNouvag 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 Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com
Phone+41718466600
Emailinfo@nouvag.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCENOU4180US0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FRNPump, Infusion

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2023-09-27
Device Publish Date2017-01-13

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