Sherlock 3CG+ TCS SR Halcyon SW Version 3.1.0 S3CG+ TCS SR Halcyon SW v3.1.0

GUDID 00801741224676

CVAD Tip Confirmation System

Bard Access Systems, Inc.

Central venous catheter navigation system, electrocardiographic/magnetic Central venous catheter navigation system, electrocardiographic/magnetic Central venous catheter navigation system, electrocardiographic/magnetic Central venous catheter navigation system, electrocardiographic/magnetic Central venous catheter navigation system, electrocardiographic/magnetic Central venous catheter navigation system, electrocardiographic/magnetic Central venous catheter navigation system, electrocardiographic/magnetic
Primary Device ID00801741224676
NIH Device Record Key220e2ad1-a17b-48b6-bf1f-269d15e83b7e
Commercial Distribution StatusIn Commercial Distribution
Brand NameSherlock 3CG+ TCS SR Halcyon SW Version 3.1.0
Version Model NumberS3CG+ TCS SR Halcyon SW v3.1.0
Catalog NumberS3CG+ TCS SR Halcyon SW v3.1.0
Company DUNS044611812
Company NameBard Access Systems, Inc.
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 Batchfalse
Serial Numbertrue
Manufacturing Datetrue
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)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com
Phone+1(800)545-0890
Emailmedical.services@crbard.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100801741224676 [Primary]

FDA Product Code

LJSCatheter, intravascular, therapeutic, long-term greater than 30 days

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-17
Device Publish Date2022-05-09

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