PATIENT CABLE-5 LEAD DU KEC022

GUDID 00841034112532

RPI

Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable
Primary Device ID00841034112532
NIH Device Record Keyf34ae445-40b9-419c-b3a1-1d42aeb8a310
Commercial Distribution StatusIn Commercial Distribution
Brand NamePATIENT CABLE-5 LEAD DU
Version Model NumberKEC022
Catalog NumberKEC022
Company DUNS066232067
Company NameRPI
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com
Phone818-882-8611
Emailtechsupport@rpiparts.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100841034112532 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DSACable, Transducer And Electrode, Patient, (Including Connector)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-12-09

On-Brand Devices [PATIENT CABLE-5 LEAD DU]

00841034112532KEC022
00841034112525KEC016
00841034112518KEC010
00841034112501KEC007
00841034112495KEC003

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