NeoLead 989803183091

GUDID 20884838035137

Philips Medical Systems

Electrocardiographic electrode, single-use
Primary Device ID20884838035137
NIH Device Record Key86741514-2933-40d3-8703-c0b88eea6442
Commercial Distribution StatusIn Commercial Distribution
Brand NameNeoLead
Version Model Number989803183091
Catalog Number989803183091
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
Emailxx@xx.xx
Phone+1(999)999-9999
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Phone+1(999)999-9999
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Phone+1(999)999-9999
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Phone+1(999)999-9999
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Phone+1(999)999-9999
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Phone+1(999)999-9999
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Phone+1(999)999-9999
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Phone+1(999)999-9999
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Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx
Phone+1(999)999-9999
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS120884838035137 [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 Date2017-04-26

On-Brand Devices [NeoLead]

20884838035182989803183141
20884838035175989803183131
20884838035168989803183121
20884838035151989803183111
20884838035144989803183101
20884838035137989803183091
20884838035106989803183081

Trademark Results [NeoLead]

Mark Image

Registration | Serial
Company
Trademark
Application Date
NEOLEAD
NEOLEAD
78461237 2998104 Live/Registered
NEOTECH PRODUCTS LLC
2004-08-03

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