Dominant Flex rack 200.4919

GUDID 07612367039642

Powered suction pump 071.0003

Medela AG

General-purpose suction system, line-powered
Primary Device ID07612367039642
NIH Device Record Key78683334-45c0-4e90-9fcc-75f7e3f96e11
Commercial Distribution StatusIn Commercial Distribution
Brand NameDominant Flex rack
Version Model NumberDominant Flex
Catalog Number200.4919
Company DUNS488293218
Company NameMedela AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com
Phone+1-877-735-1626
Emailinfo-healthcare@medela.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107612367039642 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

BTAPump, Portable, Aspiration (Manual Or Powered)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-24

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