PATIENT CABLE - 3 LD FX SN KCB002

GUDID 00841034112242

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 ID00841034112242
NIH Device Record Key4bb54371-b40c-431a-9b29-12e71d7a3fef
Commercial Distribution StatusIn Commercial Distribution
Brand NamePATIENT CABLE - 3 LD FX SN
Version Model NumberKCB002
Catalog NumberKCB002
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
GS100841034112242 [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 - 3 LD FX SN]

00841034112303KCB036
00841034112259KCB008
00841034112242KCB002

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