SpO2 Finger Adapter M-Flex 5010049

GUDID EMIP50100490

MIPM Mammendorfer Institut für Physik und Medizin GmbH

Pulse oximeter probe, reusable
Primary Device IDEMIP50100490
NIH Device Record Key57048844-f938-4eb5-98c8-89a083ad26e1
Commercial Distribution StatusIn Commercial Distribution
Brand NameSpO2 Finger Adapter M-Flex
Version Model Number5010049
Catalog Number5010049
Company DUNS324416379
Company NameMIPM Mammendorfer Institut für Physik und Medizin GmbH
Device Count5
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com
Phone+49814592090
Emailinfo@mipm.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEMIP50100490 [Direct Marking]
HIBCCEMIP50100491 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-12-02
Device Publish Date2022-11-24

On-Brand Devices [SpO2 Finger Adapter M-Flex]

EMIP501004905010049
042556292003555010049

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