Centros® CENT19K

GUDID 10884450276225

Merit Medical Systems, Inc.

Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable Double-lumen haemodialysis catheter, implantable

Primary Device ID	10884450276225
NIH Device Record Key	89380b5d-ff71-4e31-8a53-97326fd30edc
Commercial Distribution Status	In Commercial Distribution
Brand Name	Centros®
Version Model Number	00884450276228
Catalog Number	CENT19K
Company DUNS	184763290
Company Name	Merit Medical Systems, Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	true
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450276228 [Primary]
GS1	10884450276225 [Package] Contains: 00884450276228 Package: [5 Units] In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K151967

FDA Product Code

MSD	Catheter, hemodialysis, implanted

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	3
Public Version Date	2018-07-06
Device Publish Date	2016-09-20

On-Brand Devices [Centros®]

10884450276287	00884450276280
20884450276277	00884450276273
10884450276263	00884450276266
20884450276253	00884450276259
10884450276249	00884450276242
10884450276232	00884450276235
10884450276225	00884450276228
10884450276218	00884450276211
10884450276201	00884450276204
10884450276195	00884450276198
10884450276188	00884450276181
10884450276171	00884450276174
10884450242121	00884450242124
10884450242114	00884450242117
10884450242107	00884450242100
10884450242091	00884450242094
10884450242084	00884450242087
10884450242077	00884450242070
20884450242067	00884450242063
20884450242050	00884450242056
20884450242043	00884450242049
10884450242039	00884450242032
10884450242022	00884450242025
10884450242015	00884450242018

Trademark Results [Centros]

Mark Image Registration \| Serial	Company Trademark Application Date
CENTROS 77392535 3738599 Live/Registered	Radiodetection Limited 2008-02-08
CENTROS 77308729 3541404 Live/Registered	MERIT MEDICAL SYSTEMS, INC. 2007-10-19