989803149901

GUDID 20884838007806

Philips Medical Systems

Electrocardiographic electrode, single-use
Primary Device ID20884838007806
NIH Device Record Keycd6a3e4c-f682-4fc6-b8f1-f54bf82f4b58
Commercial Distribution StatusIn Commercial Distribution
Version Model Number989803149901
Catalog Number989803149901
Company DUNS078628040
Company NamePhilips Medical Systems
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(999)999-9999
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Phone+1(999)999-9999
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Device Identifiers

Device Issuing AgencyDevice ID
GS120884838007806 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DRXElectrode, electrocardiograph

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 Date2017-05-17

Devices Manufactured by Philips Medical Systems

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20884838091836 - Microstream Advance Adult-Pediatric Intubated CO2 Filter Line2021-08-02
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