PRIMOPAC CP0030

GUDID 20705032025352

PRIMO PAC ST plus F5 W/CSI

CORDIS CORPORATION

Angiographic catheter, single-use
Primary Device ID20705032025352
NIH Device Record Key506f14b2-81b2-4cdd-95d3-2ce98622006e
Commercial Distribution StatusIn Commercial Distribution
Brand NamePRIMOPAC
Version Model NumberCP0030
Catalog NumberCP0030
Company DUNS806136177
Company NameCORDIS CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
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
GS110705032025355 [Primary]
GS120705032025352 [Package]
Contains: 10705032025355
Package: Box [10 Units]
In Commercial Distribution

FDA Product Code

DQOCatheter, intravascular, diagnostic
OEZCardiovascular Procedure Kit

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-05
Device Publish Date2024-02-26

On-Brand Devices [PRIMOPAC]

20705032076729CP ST+ 6 JR4, JL4,PIG 145, CSI AVANTI, GW
20705032026137MULTIPACK INF F5
20705032025680PRIMOPACK INF F5
20705032025352PRIMO PAC ST plus F5 W/CSI

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