Home GUDID 16950900926089 INT, FirstWire
Primary DI 16950900926089
Brand INT, FirstWire
Company Shanghai Kindly Medical Instruments Co., Ltd.
Model GW353SF
Device description 0.035"*260cm, PTFE coating, straight tip
Published 2023-08-18
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name DQX Wire, Guide, Catheter
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DQX Wire, Guide, Catheter Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 16950900926089 Package GS1 10 In Commercial Distribution 26950900926086 Package GS1 40 In Commercial Distribution 46950900926080 Package GS1 160 In Commercial Distribution 56950900926087 Package GS1 100 In Commercial Distribution 06950900926082 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 16950900926089 16950900926089 26950900926086 26950900926086 46950900926080 46950900926080 56950900926087 56950900926087 06950900926082 06950900926082 6950900926082
GMDN Terms# Term, Definition table Term Definition Cardiac/peripheral vascular guidewire, single-use A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.
Regulatory Flags# DUNS number 420827639 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 true 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 06950900900693 INT,SlideCath ACJL605F1125 2023-09-11 06950900900709 INT,SlideCath ACJL606F1125 2023-09-11 06950900900716 INT,SlideCath ACJR304F1100 2023-09-11 06950900900723 INT,SlideCath ACJR307F1100 2023-09-11 06950900900730 INT,SlideCath ACJR355F1125 2023-09-11 06950900900747 INT,SlideCath ACJR356F1125 2023-09-11 06950900900754 INT,SlideCath ACJR405F1125 2023-09-11 06950900900761 INT,SlideCath ACJR406F1125 2023-09-11 06950900900778 INT,SlideCath ACJR455F1100 2023-09-11 06950900900785 INT,SlideCath ACJR456F1100 2023-09-11 06950900900792 INT,SlideCath ACJR456F1125 2023-09-11 06950900900808 INT,SlideCath ACJR457F1100 2023-09-11 06950900900815 INT,SlideCath ACJR505F1125 2023-09-11 06950900900822 INT,SlideCath ACJR506F1125 2023-09-11 06950900900839 INT,SlideCath ACJR605F1125 2023-09-11 06950900900846 INT,SlideCath ACJR606F1125 2023-09-11 06950900900853 INT,SlideCath ACTIG24F1100 2023-09-11 06950900900860 INT,SlideCath ACTIG25F1100 2023-09-11 06950900900877 INT,SlideCath ACTIG27F1100 2023-09-11 06950900900884 INT,SlideCath ACTIG34F1100 2023-09-11
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