Patient Cables

GUDID 90817266020542

Patient Cable Non Detachable 5 Lead

MERIT CABLES INCORPORATED

Electrocardiographic lead set, reusable
Primary Device ID90817266020542
NIH Device Record Key6f7be101-d125-435b-8822-42026cdae466
Commercial Distribution StatusIn Commercial Distribution
Brand NamePatient Cables
Version Model Number425XX
Company DUNS180587883
Company NameMERIT CABLES INCORPORATED
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com
Phone714-918-1935
Emailrmauricio@meritcables.com

Device Dimensions

Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet
Length14 Feet
Length13 Feet

Device Identifiers

Device Issuing AgencyDevice ID
GS190817266020542 [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 Date2016-09-23

On-Brand Devices [Patient Cables]

908172660208325 Lead Patient Trunk Cable
90817266020542Patient Cable Non Detachable 5 Lead

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.