Nikomed ECG Cable 3603

GUDID 00853512006745

3 Lead Monitor Cable

NIKOMED USA

Electrical-only medical device connection cable, reusable
Primary Device ID00853512006745
NIH Device Record Key05686a35-bda0-491a-be8f-b099326f1b40
Commercial Distribution StatusIn Commercial Distribution
Brand NameNikomed ECG Cable
Version Model Number3603
Catalog Number3603
Company DUNS073648341
Company NameNIKOMED USA
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
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+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com
Phone+1(800)355-6456
Emailinfo@nikomedusa.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100853512006745 [Primary]

FDA Product Code

IKDCable, Electrode

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-29
Device Publish Date2021-01-21

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