ReSolve ConvertX® RCX12-8-038

GUDID 10884450452865

Merit Medical Systems, Inc.

Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent Polymeric ureteral stent
Primary Device ID10884450452865
NIH Device Record Key1d741713-bfcc-46ed-8f95-1780852f21fd
Commercial Distribution StatusIn Commercial Distribution
Brand NameReSolve ConvertX®
Version Model Number00884450452868
Catalog NumberRCX12-8-038
Company DUNS184763290
Company NameMerit Medical Systems, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100884450452868 [Primary]
GS110884450452865 [Package]
Contains: 00884450452868
Package: [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FADStent, ureteral

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-02-05
Device Publish Date2020-01-28

On-Brand Devices [ReSolve ConvertX®]

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1088445072154100884450721544
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1088445072119000884450721193
10884450721527C
10884450721282C
10884450721237C
10884450721312C
10884450721244C
10884450721213C

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