NeoLead N301

GUDID 10812594011051

Electrode (Box of 20)

NEOTECH PRODUCTS, INC.

Electrocardiographic electrode, single-use
Primary Device ID10812594011051
NIH Device Record Keye238d795-f40c-4277-8d0d-0f2b5163251f
Commercial Distribution StatusIn Commercial Distribution
Brand NameNeoLead
Version Model Number10812594011051
Catalog NumberN301
Company DUNS198013435
Company NameNEOTECH PRODUCTS, INC.
Device Count50
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100812594011047 [Unit of Use]
GS110812594011051 [Primary]

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 Date2021-06-14
Device Publish Date2016-09-14

On-Brand Devices [NeoLead]

00812594011054812594011054
10812594011051Electrode (Box of 20)

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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