Cordis PRECISE RX Nitinol Stent System P07030RXC

GUDID 20705032035306

CORDIS CORPORATION

Bare-metal carotid artery stent
Primary Device ID20705032035306
NIH Device Record Keyd2cafd5d-c0d6-4012-8cea-3950aab35cf3
Commercial Distribution StatusIn Commercial Distribution
Brand NameCordis PRECISE RX Nitinol Stent System
Version Model NumberP07030RXC
Catalog NumberP07030RXC
Company DUNS806136177
Company NameCORDIS CORPORATION
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS120705032035306 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NIMSTENT, CAROTID

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-02-11
Device Publish Date2014-09-17

On-Brand Devices [Cordis PRECISE RX Nitinol Stent System]

20705032035610P10020RXC
20705032035559P09030RXC
20705032035528P09020RXC
20705032035450P08040RXC
20705032035429P08030RXC
20705032035399P08020RXC
20705032035337P07040RXC
20705032035306P07030RXC
20705032035276P07020RXC
20705032035214P06040RXC
20705032035184P06030RXC
20705032035153P06020RXC
20705032035092P05040RXC
20705032035030P05020RXC

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