Home GUDID 20705032002407 MAXI LD
Primary DI 20705032002407
Brand MAXI LD
Company Cordis US Corp.
Model 4162540S
Catalog number 4162540S
Device description MAXI LD 7F 25X4 80CM
Published 2016-08-01
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true Product Codes# Code, Name table Code Name LIT Catheter, angioplasty, peripheral, transluminal
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LIT Catheter, Angioplasty, Peripheral, Transluminal Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 20705032002407 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 20705032002407 20705032002407
GMDN Terms# Term, Definition table Term Definition Peripheral angioplasty balloon catheter, basic A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include microsurgical blades (atherotomes) to score the plaque. This is a single-use device.
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Do not use if package is damanged Special Storage Condition, Specify 0 0 Store in cool, dark, dry place Storage Environment Temperature 15 Degrees Celsius 30 Degrees Celsius
Regulatory Flags# DUNS number 118274128 Device count 1 Lot or batch true Expiration date on label true No natural rubber latex true 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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