Home GUDID 26950900952580 INT or KDL
Primary DI 26950900952580
Brand INT or KDL
Company Shanghai Kindly Medical Instruments Co., Ltd.
Model IS02A
Device description Interventional radiology percutaneous-access procedure kit.
Published 2023-06-01
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 DYB Introducer, Catheter
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DYB Introducer, Catheter Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 26950900952580 Package GS1 5 In Commercial Distribution 46950900952584 Package GS1 200 In Commercial Distribution 06950900952586 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 26950900952580 26950900952580 46950900952584 46950900952584 06950900952586 06950900952586 6950900952586
GMDN Terms# Term, Definition table Term Definition Interventional radiology percutaneous-access kit, single-use A collection of various instruments/devices (e.g., introducer sheath, dilator, guides, cannula, needle, angiographic catheter) intended to be used for percutaneous body-access to facilitate a radiological image-guided interventional radiology or surgical procedure [e.g., bile duct biopsy, percutaneous transhepatic cholangiogram, non-vascular drainage procedures, ultrasound-guided spinal surgery]. Some types are designed to function as a channel to facilitate the introduction of radiological image guidance devices (e.g., ultrasound probe/transducer) [not included]. It does not contain pharmaceuticals. 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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