Home GUDID 17290018072001 Bendit2.7 Steerable Microcatheter
Primary DI 17290018072001
Brand Bendit2.7 Steerable Microcatheter
Company BEND IT TECHNOLOGIES LTD
Model BDT01200
Device description The Bendit2.7™ Steerable Microcatheter is intended for general intravascular use in the peripheral vasculature. The microcatheter can be used for the delivery of diagnostic, embolic, or therapeutic materials into the vasculature.
Published 2020-08-24
Public version status New
Distribution status In Commercial Distribution
MRI safety MR Unsafe
Rx true
Sterile true
Single use true
Product Codes# Code, Name table Code Name KRA Catheter, Continuous Flush
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KRA Catheter, Continuous Flush Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 27290018072008 Package GS1 1 In Commercial Distribution 37290018072005 Package GS1 3 In Commercial Distribution 47290018072002 Package GS1 5 In Commercial Distribution 57290018072009 Package GS1 10 In Commercial Distribution 17290018072001 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 27290018072008 27290018072008 37290018072005 37290018072005 47290018072002 47290018072002 57290018072009 57290018072009 17290018072001 17290018072001
GMDN Terms# Term, Definition table Term Definition Vascular microcatheter A sterile, small-diameter, single-lumen, flexible tube designed for the controlled infusion of fluids (e.g., thrombolytics, diagnostic contrast media) into superselective small vessels (including intracranial, peripheral, or occluded coronary vasculature) for angiography/treatment, and typically also for the delivery of devices (e.g., embolization implants, guidewires) into tortuous vessels or across tight lesions. It may include an ultrasound transducer, a thermal sensor, and a hole for guidewire placement located at the distal tip. It is not a guide-catheter (i.e., is not intended to deliver other catheters or therapeutic leads directly through its lumen). This is a single-use device.
Regulatory Flags# DUNS number 600476669 Device count 1 Lot or batch true Serial number true Manufacturing date on label true Expiration date on label true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 17290018072049 Bendit®21 Microcatheter BDT21157U2 2022-06-09
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