Narcotrend Electrode

GUDID 04260497026006

MT MonitorTechnik GmbH & Co. KG

Electrocardiographic electrode, single-use
Primary Device ID04260497026006
NIH Device Record Key17e1ad2b-227d-4d01-b2fe-d2b83a70b73a
Commercial Distribution StatusIn Commercial Distribution
Brand NameNarcotrend Electrode
Version Model NumberEE-0203
Company DUNS388136913
Company NameMT MonitorTechnik GmbH & Co. KG
Device Count25
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+494192201753
Emailinfo@monitortechnik.de

Device Identifiers

Device Issuing AgencyDevice ID
GS104260497026006 [Primary]
GS104260497026013 [Package]
Package: [10 Units]
In Commercial Distribution
GS104260497026075 [Unit of Use]
GS104260497026082 [Package]
Contains: 04260497026013
Package: Carton [12 Units]
In Commercial Distribution

FDA Product Code

DRXElectrode, Electrocardiograph

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-03-26
Device Publish Date2018-05-15

Devices Manufactured by MT MonitorTechnik GmbH & Co. KG

04260497021063 - Narcotrend-Compact M2019-03-26
04260497026006 - Narcotrend Electrode2019-03-26
04260497026006 - Narcotrend Electrode2019-03-26
04260497025009 - Narcotrend Patient lead2018-07-06 1-channel (3 electrodes) Component of Narcotrend-Compact M (Primary DI Number: 04260497021063)
04260497025016 - Narcotrend Patient lead2018-07-06 2-channel (4 electrodes) Component of Narcotrend-Compact M (Primary DI Number: 04260497021063)

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.