Home GUDID 20705032100073 INFINITI™ AMBI
Primary DI 20705032100073
Brand INFINITI™ AMBI
Company Cordis US Corp.
Model 555525J402
Catalog number 555525J402
Device description 5F INFINITI AMBI 125CM JK 4.0
Published 2024-02-16
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name DQO Catheter, intravascular, diagnostic
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DQO Catheter, Intravascular, Diagnostic Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 20705032100073 Package GS1 5 In Commercial Distribution 10705032100076 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 20705032100073 20705032100073 10705032100076 10705032100076
GMDN Terms# Term, Definition table Term Definition Angiographic catheter, single-use A thin, flexible tube designed to inject a contrast medium into select blood vessels of the cerebral, visceral, or peripheral vasculature during an angiographic procedure in order to facilitate the clear visualization of the vascular system of a targeted organ or area of the body. It is introduced percutaneously, has a radiopaque marker(s) for positioning, and may include disposable devices dedicated to catheter introduction/function [e.g., sheath(s)]. It may also be used for simultaneous pressure measurements to determine the transvalvular, intravascular, and intraventricular pressure gradients. This is a single-use device.
Regulatory Flags# DUNS number 118274128 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 10705032057004 AQUATRACK™ Hydrophilic Nitinol Guidewire C3515RSA C3515RSA 2026-07-29 10705032057011 AQUATRACK™ Hydrophilic Nitinol Guidewire C3515RSS C3515RSS 2026-07-29 10705032057028 AQUATRACK™ Hydrophilic Nitinol Guidewire C3515SSA C3515SSA 2026-07-29 10705032057035 AQUATRACK™ Hydrophilic Nitinol Guidewire C3518RSA C3518RSA 2026-07-29 10705032057042 AQUATRACK™ Hydrophilic Nitinol Guidewire C3518RSS C3518RSS 2026-07-29 10705032057059 AQUATRACK™ Hydrophilic Nitinol Guidewire C3518SSA C3518SSA 2026-07-29 10705032057066 AQUATRACK™ Hydrophilic Nitinol Guidewire C3526RSA C3526RSA 2026-07-29 10705032057073 AQUATRACK™ Hydrophilic Nitinol Guidewire C3526SSA C3526SSA 2026-07-29 10705032057080 AQUATRACK™ Hydrophilic Nitinol Guidewire C3526SSS C3526SSS 2026-07-29 10705032100656 VISTA BRITE TIP 778-052-00M 778-052-00M 2024-09-09 10705032100663 VISTA BRITE TIP 778-082-00M 778-082-00M 2024-09-09 10705032100748 VISTA BRITE TIP 670-190-00M 670-190-00M 2024-09-09 10705032100830 VISTA BRITE TIP 670-040-00M 670-040-00M 2024-09-09 10705032100892 VISTA BRITE TIP 778-034-00M 778-034-00M 2024-09-09 10705032100922 VISTA BRITE TIP 670-008-00M 670-008-00M 2024-09-09 10705032100953 VISTA BRITE TIP 778-270-00M 778-270-00M 2024-09-09 10862028000434 MYNX CONTROL MX6760 MX6760 2018-10-22 10862028000427 MYNX CONTROL MX5060 MX5060 2018-10-22 20705032036440 Cordis PRECISE PRO Rx Nitinol Stent System PC0720RXC PC0720RXC 2014-09-17 10705032009768 AVANTI 504405X 504405X 2016-08-01
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